The intrauterine devices are a safe, reliable, long-acting and reversible contraceptive method. It is also sound safe and cheap contraceptive methods available and is nearly maintenance free for up to 10 years. The fear and the pain associated with intrauterine devices insertion consider barriers to using this contraception method, this is because that the mucosal lining of female genital tract is highly sensitive to touch and pain. However; most of small procedures done in this sensitive area are performed without analgesia. The pain during intrauterine devices insertion is due to application of the tenaculum , traction of the cervical canal, passing the uterine sound, insertion of the intrauterine devices through the cervix, and irritation of the endometrial lining by the intrauterine devices . Previous studies have reported different lines to decrease pain during intrauterine device insertion starting by simple methods such as pre-insertion ibuprofen use, intracervical or intrauterine lidocaine and misoprostol up to paracervical blocks. Previous studies, in literature, have found that the most painful steps during intrauterine devices insertion were uterine sounding then intrauterine device insertion itself, followed by tenaculum placement. One recent study addressed pain effect using an atraumatic vulsellum and a single-tooth tenaculum on pain perception during intrauterine devices and found no difference in reported pain.

NCT02842177

Conditions

1. Contraception

Interventions

1. Procedure: Classic group
2. Procedure: Uterine sounding sparing group
3. Radiation: Transvaginal ultrasound
4. Device: Cu-IUD

Classic vs. Uterine Sound-sparing Approach for Insertion of Copper T380A Intrauterine Device. --- T380A ---

The purpose of this multi-center clinical trial is to evaluate the safety and effectiveness of inserting an intrauterine device (IUD) immediately after a suction aspiration procedure compared to inserting the IUD 2-6 weeks after the procedure. This study will also evaluate how satisfied women are with the timing of their IUD placement. Subjects will be able to choose between the Paraguard IUD or the Mirena IUD. The researchers hypothesize that: 1. the expulsion rates measured at 1, 3 and 6 months will be clinically equivalent with immediate insertion compared with delayed insertion, 2. satisfaction and tolerance of side effects will be higher with immediate IUD insertion compared with delayed insertion, and 3. overall IUD use/continuation rates measured at 1, 3 and 6 months will be higher with immediate IUD insertion compared with delayed insertion.

NCT00562276

Conditions

1. Contraception

Interventions

1. Procedure: Immediate IUD insertion

laminaria) or misoprostol for cervical preparation during the aspiration procedure - Allergy to polyethylene - Allergy to levonorgestrel (for levonorgestrel-containing IUS only) - Allergy to copper (for copper T380A IUD only) - Wilson's disease (for copper T380A IUD only) - Current participation in another research study which would interfere with the conduct of this study Inclusion Criteria: - Female - 18 years or older - Requesting suction aspiration for spontaneous or elective abortion - Intrauterine pregnancy documented with ultrasound. --- T380A ---

laminaria) or misoprostol for cervical preparation during the aspiration procedure - Allergy to polyethylene - Allergy to levonorgestrel (for levonorgestrel-containing IUS only) - Allergy to copper (for copper T380A IUD only) - Wilson's disease (for copper T380A IUD only) - Current participation in another research study which would interfere with the conduct of this study Inclusion Criteria: - Female - 18 years or older - Requesting suction aspiration for spontaneous or elective abortion - Intrauterine pregnancy documented with ultrasound. --- T380A --- --- T380A ---

laminaria) or misoprostol for cervical preparation during the aspiration procedure - Allergy to polyethylene - Allergy to levonorgestrel (for levonorgestrel-containing IUS only) - Allergy to copper (for copper T380A IUD only) - Wilson's disease (for copper T380A IUD only) - Current participation in another research study which would interfere with the conduct of this study Contraception null --- T380A ---

laminaria) or misoprostol for cervical preparation during the aspiration procedure - Allergy to polyethylene - Allergy to levonorgestrel (for levonorgestrel-containing IUS only) - Allergy to copper (for copper T380A IUD only) - Wilson's disease (for copper T380A IUD only) - Current participation in another research study which would interfere with the conduct of this study Contraception null --- T380A --- --- T380A ---

The purpose of this study is to see if women presenting for emergency contraception (EC) and choose the copper intrauterine device (IUD) will have fewer unplanned pregnancies in the next year compared to women who choose oral levonorgestrel for EC. The study will also compare use of an effective method of contraception in the year after they received EC.

NCT00966771

Conditions

1. Pregnancy

Interventions

1. Drug: Copper T380 IUD
2. Drug: Oral levonorgestrel

MeSH:Emergencies

The Copper T380A IUD vs. Oral Levonorgestrel for Emergency Contraception The purpose of this study is to see if women presenting for emergency contraception (EC) and choose the copper intrauterine device (IUD) will have fewer unplanned pregnancies in the next year compared to women who choose oral levonorgestrel for EC. --- T380A ---

The purpose of this study is to compare delayed vs. immediate insertion of the Copper T 380 IUD after termination of pregnancy after 12 weeks.

NCT00540046

Conditions

1. Contraception Behavior

Interventions

1. Device: Copper T 380A IUD

Number of participants using Copper T380A IUD 6 months after surgery. --- T380A ---

This study is designed to evaluate if self-inserted intravaginal 2% lidocaine gel is effective at decreasing pain during intrauterine device insertion in nulliparous women.

NCT01534520

Conditions

1. Pain

Interventions

1. Drug: Lidocaine
2. Drug: Placebo

Inclusion criteria: - Nulliparous, as defined in this study as no history of pregnancy ≥ 24 weeks gestational age - Desires insertion of either levonorgestrel-releasing IUD (LNG-IUD) or copper T380A IUD (Cu-IUD) - No history of pregnancy in the last 6 weeks - Able to provide written informed consent in English and comply with all study procedures Exclusion criteria: - Known allergy or hypersensitivity to lidocaine or other amino amide local anesthetics - Prior failed IUD insertion - Prior IUD use - Use of narcotic or benzodiazepine medication within the last 24 hours - U.S. Centers for Disease Control Medical Eligibility Criteria (MEC) category 3 or 4 classification for use of an IUD - Positive pregnancy test or reasonable risk of pregnancy due to unprotected heterosexual intercourse since the last menstrual period Inclusion criteria: - Nulliparous, as defined in this study as no history of pregnancy ≥ 24 weeks gestational age - Desires insertion of either levonorgestrel-releasing IUD (LNG-IUD) or copper T380A IUD (Cu-IUD) - No history of pregnancy in the last 6 weeks - Able to provide written informed consent in English and comply with all study procedures Exclusion criteria: - Known allergy or hypersensitivity to lidocaine or other amino amide local anesthetics - Prior failed IUD insertion - Prior IUD use - Use of narcotic or benzodiazepine medication within the last 24 hours - U.S. Centers for Disease Control Medical Eligibility Criteria (MEC) category 3 or 4 classification for use of an IUD - Positive pregnancy test or reasonable risk of pregnancy due to unprotected heterosexual intercourse since the last menstrual period Pain Intrauterine devices (IUDs) are among the most effective forms of reversible contraception. --- T380A ---

Inclusion criteria: - Nulliparous, as defined in this study as no history of pregnancy ≥ 24 weeks gestational age - Desires insertion of either levonorgestrel-releasing IUD (LNG-IUD) or copper T380A IUD (Cu-IUD) - No history of pregnancy in the last 6 weeks - Able to provide written informed consent in English and comply with all study procedures Exclusion criteria: - Known allergy or hypersensitivity to lidocaine or other amino amide local anesthetics - Prior failed IUD insertion - Prior IUD use - Use of narcotic or benzodiazepine medication within the last 24 hours - U.S. Centers for Disease Control Medical Eligibility Criteria (MEC) category 3 or 4 classification for use of an IUD - Positive pregnancy test or reasonable risk of pregnancy due to unprotected heterosexual intercourse since the last menstrual period Inclusion criteria: - Nulliparous, as defined in this study as no history of pregnancy ≥ 24 weeks gestational age - Desires insertion of either levonorgestrel-releasing IUD (LNG-IUD) or copper T380A IUD (Cu-IUD) - No history of pregnancy in the last 6 weeks - Able to provide written informed consent in English and comply with all study procedures Exclusion criteria: - Known allergy or hypersensitivity to lidocaine or other amino amide local anesthetics - Prior failed IUD insertion - Prior IUD use - Use of narcotic or benzodiazepine medication within the last 24 hours - U.S. Centers for Disease Control Medical Eligibility Criteria (MEC) category 3 or 4 classification for use of an IUD - Positive pregnancy test or reasonable risk of pregnancy due to unprotected heterosexual intercourse since the last menstrual period Pain Intrauterine devices (IUDs) are among the most effective forms of reversible contraception. --- T380A --- --- T380A ---

This study aims to use validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD.

NCT02311478

Conditions

1. Intrauterine Devices, Copper
2. Metrorrhagia
3. Menstruation
4. Menstrual Cycle

Interventions

1. Device: T380A Intrauterine Copper Contraceptive

MeSH:Metrorrhagia Hemorrhage

HPO:Metrorrhagia

Tracking IUD Bleeding Experiences: An Evaluation of Bleeding Profiles in New Intrauterine Device Users This study aims to use validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD. --- T380A ---

Women will track bleeding after the insertion of the T380A IUD for 180 days. --- T380A ---

Participants will be contacted monthly to collect data.. Assess the Relationship of Menstrual Cycle Changes Among Women Initiating the Copper T380 IUD to Method Satisfaction and Continuation at 6 Months Post Insertion.. Determine rates of continuation and level of satisfaction with the IUD during the first 6 months of use.. Inclusion Criteria: - Healthy women ages 18-40 years with regular, normal menses (lasting between 3-7 days) and who are initiating an IUD - Women who can provide bleeding information for 3 cycles off of any hormonal contraception (or non-hormonal IUD) and are willing to track bleeding for 180 days - Women who are between 6 and 12 months postpartum (if they have had normal menses the last 3 cycles) Exclusion Criteria: - Use of any hormonal contraceptive method in the previous 3 months - Irregular duration of menstrual cycles in the last 3 cycles (<21 or >35 days) - Recent history of menstrual bleeding lasting less than 3 days or greater than 7 days based on self report of the last 3 cycles - Contraindication to use of the ParaGard® T380A IUD - Mucopurulent cervicitis at the time of IUD insertion - Unable to speak, read, and write in English - Currently pregnant - Plans for or desire for pregnancy in the next 6 months - Currently breastfeeding - Women who are <6 months postpartum - Participation in any clinical investigation utilizing an investigational drug or medical device or requiring invasive gynecologic procedures within the 30 days prior to enrollment - Wilson's disease - Known coagulopathy or bleeding disorder Inclusion Criteria: - Healthy women ages 18-40 years with regular, normal menses (lasting between 3-7 days) and who are initiating an IUD - Women who can provide bleeding information for 3 cycles off of any hormonal contraception (or non-hormonal IUD) and are willing to track bleeding for 180 days - Women who are between 6 and 12 months postpartum (if they have had normal menses the last 3 cycles) Exclusion Criteria: - Use of any hormonal contraceptive method in the previous 3 months - Irregular duration of menstrual cycles in the last 3 cycles (<21 or >35 days) - Recent history of menstrual bleeding lasting less than 3 days or greater than 7 days based on self report of the last 3 cycles - Contraindication to use of the ParaGard® T380A IUD - Mucopurulent cervicitis at the time of IUD insertion - Unable to speak, read, and write in English - Currently pregnant - Plans for or desire for pregnancy in the next 6 months - Currently breastfeeding - Women who are <6 months postpartum - Participation in any clinical investigation utilizing an investigational drug or medical device or requiring invasive gynecologic procedures within the 30 days prior to enrollment - Wilson's disease - Known coagulopathy or bleeding disorder Intrauterine Devices, Copper Metrorrhagia Menstruation Menstrual Cycle Metrorrhagia Hemorrhage New users of the intrauterine device (IUD) are most likely to discontinue use within the first six months after insertion. --- T380A ---

Participants will be contacted monthly to collect data.. Assess the Relationship of Menstrual Cycle Changes Among Women Initiating the Copper T380 IUD to Method Satisfaction and Continuation at 6 Months Post Insertion.. Determine rates of continuation and level of satisfaction with the IUD during the first 6 months of use.. Inclusion Criteria: - Healthy women ages 18-40 years with regular, normal menses (lasting between 3-7 days) and who are initiating an IUD - Women who can provide bleeding information for 3 cycles off of any hormonal contraception (or non-hormonal IUD) and are willing to track bleeding for 180 days - Women who are between 6 and 12 months postpartum (if they have had normal menses the last 3 cycles) Exclusion Criteria: - Use of any hormonal contraceptive method in the previous 3 months - Irregular duration of menstrual cycles in the last 3 cycles (<21 or >35 days) - Recent history of menstrual bleeding lasting less than 3 days or greater than 7 days based on self report of the last 3 cycles - Contraindication to use of the ParaGard® T380A IUD - Mucopurulent cervicitis at the time of IUD insertion - Unable to speak, read, and write in English - Currently pregnant - Plans for or desire for pregnancy in the next 6 months - Currently breastfeeding - Women who are <6 months postpartum - Participation in any clinical investigation utilizing an investigational drug or medical device or requiring invasive gynecologic procedures within the 30 days prior to enrollment - Wilson's disease - Known coagulopathy or bleeding disorder Inclusion Criteria: - Healthy women ages 18-40 years with regular, normal menses (lasting between 3-7 days) and who are initiating an IUD - Women who can provide bleeding information for 3 cycles off of any hormonal contraception (or non-hormonal IUD) and are willing to track bleeding for 180 days - Women who are between 6 and 12 months postpartum (if they have had normal menses the last 3 cycles) Exclusion Criteria: - Use of any hormonal contraceptive method in the previous 3 months - Irregular duration of menstrual cycles in the last 3 cycles (<21 or >35 days) - Recent history of menstrual bleeding lasting less than 3 days or greater than 7 days based on self report of the last 3 cycles - Contraindication to use of the ParaGard® T380A IUD - Mucopurulent cervicitis at the time of IUD insertion - Unable to speak, read, and write in English - Currently pregnant - Plans for or desire for pregnancy in the next 6 months - Currently breastfeeding - Women who are <6 months postpartum - Participation in any clinical investigation utilizing an investigational drug or medical device or requiring invasive gynecologic procedures within the 30 days prior to enrollment - Wilson's disease - Known coagulopathy or bleeding disorder Intrauterine Devices, Copper Metrorrhagia Menstruation Menstrual Cycle Metrorrhagia Hemorrhage New users of the intrauterine device (IUD) are most likely to discontinue use within the first six months after insertion. --- T380A --- --- T380A ---

This study aims to incorporate these validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD. --- T380A ---

To investigate whether vaginal dinoprostone administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications and pain in nulliparous women.

NCT03686085

Conditions

1. Intrauterine Device

Interventions

1. Drug: Dinoprostone 3 mg
2. Drug: placebo vaginal tablet

Effects of Prophylactic Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women.. Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women. --- T380A ---

Effects of Prophylactic Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women.. Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women. --- T380A --- --- T380A ---

The purpose of this study is to determine the expulsion rates of copper Intrauterine Devices (IUDs) placed at time of Cesarean Delivery.

NCT01439802

Conditions

1. Intrauterine Device Expulsion

Interventions

1. Device: Copper IUD placement at time Cesarean Delivery (Copper T 380A)

After delivery of the placenta, a ParaGard® copper T380A IUD was inserted through the hysterotomy site. --- T380A ---

Intrauterine devices (IUDs) are an effective form of contraception, but only about 3.4% of women in the US report using them. Women must often wait for their menses to start, or for results of screening for sexually transmitted infections (STIs), before their doctors will place IUDs for them. This is not the case with other birth control methods. Researchers know that it is safe to start oral contraceptive pills, transdermal patches or vaginal rings on the same day of a doctor's visit. In the investigators clinical practice, the investigators often place IUDs on the same day of a woman's visit, but outcomes have not been formally assessed. Currently, there are two kinds of IUDs available in the United States: the ParaGard T380A and the Mirena levonorgestrel intrauterine system (LNG-IUS). The investigators want to know if women who have IUDs placed at any time during their menstrual cycle have different experiences regarding the following, compared to those who have IUDS placed during the first 7 days of their cycle: bleeding or cramping patterns, active pelvic infections, becoming pregnant more often during that first cycle (window pregnancy). Women who come to their provider seeking an IUD for birth control will be asked to participate in this study. The investigators will ask them to keep track of their bleeding and cramping for three subsequent months to see if patterns differ according to the day in their menstrual cycle that the device was inserted. They will be randomly assigned either to record this information on paper, or to send in the information by responding to daily text messages. The investigators want to know if women who have an IUD placed at any time during the menstrual cycle have different outcomes compared to those who have IUDs placed during the first 7 days of their cycle. If the investigators have this information, the investigators can make recommendations to physicians, help counsel patients, and potentially expand access to IUDs.

NCT01730911

Conditions

1. Bleeding
2. Cramping
3. Pregnancy With IUD in Place
4. IUD Expulsion
5. IUD Removal

Interventions

1. Other: Text message

MeSH:Muscle Cramp Spasm Hemorrhage

HPO:Hyperkinetic movements Muscle spasm

Currently, there are two kinds of IUDs available in the United States: the ParaGard T380A and the Mirena levonorgestrel intrauterine system (LNG-IUS). --- T380A ---

Women who have just given birth are at high risk for rapid repeat pregnancy, which can lead to negative consequences during the subsequent pregnancy. Providers have traditionally delayed starting birth control, especially placement of intrauterine devices (IUDs), post-delivery for a number of reasons. The first postpartum visit after a woman has given birth is typically scheduled for 6 weeks after her delivery, during which she is typically provided with her chosen method of birth control. This study will evaluate two different IUD placement times: 3 weeks and 6 weeks after delivery. This will allow the researchers to determine if placement time affects a woman's follow-through obtaining the IUD and keeping it inserted in place. The researchers will also look at bleeding patterns and patient/provider satisfaction with the IUD placement

NCT01594476

Conditions

1. Contraception

Interventions

1. Drug: Levonorgestrel IUS

The distance from the left side of the 10 cm line to the mark will be measured in millimeters and compared between randomization groups if they received an IUD at the allocated timing of 18-24 or 39-45 days.. Inclusion Criteria: - Female - 18 years or older - Voluntarily requesting either copper T380A or levonorgestrel IUD placement for postpartum contraception - Within 5 days of vaginal or cesarean delivery of live born infant ≥32 0/7 weeks at the time of enrollment - English or Spanish speaking - Able to give consent and agree to terms of the study - No contraindications to use of either intrauterine device Exclusion Criteria: - Preterm delivery prior to 32 weeks gestation - Recent pregnancy with multiple gestation - Current incarceration - Known congenital or acquired uterine anomaly, including fibroids that distort the uterine cavity - Current or recent pelvic infection (chorioamnionitis treated for fever in labor only is not an exclusion) - Suspected hypersensitivity or contraindication to the chosen IUD - No insurance coverage for postpartum care, including Citizen Alien Waived Emergent Medical (CAWEM) Inclusion Criteria: - Female - 18 years or older - Voluntarily requesting either copper T380A or levonorgestrel IUD placement for postpartum contraception - Within 5 days of vaginal or cesarean delivery of live born infant ≥32 0/7 weeks at the time of enrollment - English or Spanish speaking - Able to give consent and agree to terms of the study - No contraindications to use of either intrauterine device Exclusion Criteria: - Preterm delivery prior to 32 weeks gestation - Recent pregnancy with multiple gestation - Current incarceration - Known congenital or acquired uterine anomaly, including fibroids that distort the uterine cavity - Current or recent pelvic infection (chorioamnionitis treated for fever in labor only is not an exclusion) - Suspected hypersensitivity or contraindication to the chosen IUD - No insurance coverage for postpartum care, including Citizen Alien Waived Emergent Medical (CAWEM) Contraception The goal of this study is to investigate whether early interval placement of a postpartum IUD at 3 weeks postpartum, compared to the usual 6 weeks postpartum, is associated with greater uptake of the IUD by 3 months after delivery. --- T380A ---

The distance from the left side of the 10 cm line to the mark will be measured in millimeters and compared between randomization groups if they received an IUD at the allocated timing of 18-24 or 39-45 days.. Inclusion Criteria: - Female - 18 years or older - Voluntarily requesting either copper T380A or levonorgestrel IUD placement for postpartum contraception - Within 5 days of vaginal or cesarean delivery of live born infant ≥32 0/7 weeks at the time of enrollment - English or Spanish speaking - Able to give consent and agree to terms of the study - No contraindications to use of either intrauterine device Exclusion Criteria: - Preterm delivery prior to 32 weeks gestation - Recent pregnancy with multiple gestation - Current incarceration - Known congenital or acquired uterine anomaly, including fibroids that distort the uterine cavity - Current or recent pelvic infection (chorioamnionitis treated for fever in labor only is not an exclusion) - Suspected hypersensitivity or contraindication to the chosen IUD - No insurance coverage for postpartum care, including Citizen Alien Waived Emergent Medical (CAWEM) Inclusion Criteria: - Female - 18 years or older - Voluntarily requesting either copper T380A or levonorgestrel IUD placement for postpartum contraception - Within 5 days of vaginal or cesarean delivery of live born infant ≥32 0/7 weeks at the time of enrollment - English or Spanish speaking - Able to give consent and agree to terms of the study - No contraindications to use of either intrauterine device Exclusion Criteria: - Preterm delivery prior to 32 weeks gestation - Recent pregnancy with multiple gestation - Current incarceration - Known congenital or acquired uterine anomaly, including fibroids that distort the uterine cavity - Current or recent pelvic infection (chorioamnionitis treated for fever in labor only is not an exclusion) - Suspected hypersensitivity or contraindication to the chosen IUD - No insurance coverage for postpartum care, including Citizen Alien Waived Emergent Medical (CAWEM) Contraception The goal of this study is to investigate whether early interval placement of a postpartum IUD at 3 weeks postpartum, compared to the usual 6 weeks postpartum, is associated with greater uptake of the IUD by 3 months after delivery. --- T380A --- --- T380A ---

Subjects will choose to receive either a levonorgestrel-containing IUS (Mirena) or copper T380A IUD (ParaGard). --- T380A ---

The study will be a randomized clinical trial. Women with less than 10 prenatal visits and/or 2 or more no show visits who desire an Intrauterine Device (IUD) will be considered for enrollment. If consented and meet inclusion criteria, they will be randomized after delivery to receive an IUD immediately postplacental or at their routine postpartum visit. Women who plan to deliver a live birth singleton via vaginal or cesarean delivery at Oregon Health and Science University (OHSU) hospital will be considered for inclusion in the study. Women who desire an IUD for postpartum contraception will be approached for study participation. The postpartum contraception plan is routinely documented during their prenatal course. It is also addressed by the obstetrical team upon admission to Labor & Delivery at OHSU. The obstetrical team will identify subjects who present in labor who meet the criteria of poor prenatal clinic attendance and express interest in intrauterine contraception. Immediately after vaginal or cesarean delivery, consented subjects will be randomized to immediate postplacental IUD placement or IUD placement at their routine postpartum visit. Women randomized to the immediate postplacental IUD group will receive their IUD within 60 minutes of placental delivery. Prior to discharge from the hospital women who received a postplacental IUD will be assisted in scheduling a routine postpartum visit with their primary provider. Subjects who are randomized for IUD insertion at their postpartum visit will be assisted in scheduling a postpartum visit and IUD placement with their usual obstetrical care provider. All subjects in the delayed group will be provided with contact information for the Women's Health Research Unit (WHRU) at OHSU. If a subject cannot obtain an IUD at her usual place of care, the device will be placed at no cost through the WHRU. At 3 months after delivery, all subjects will be contacted by phone, text, or email to complete a questionnaire to determine whether they have had a known expulsion, pregnancy, or elective IUD removal. The questionnaire will include questions regarding ease of placement and overall satisfaction with the timing of placement. Subjects will be compensated for their participation in the study after the 3 month contact.

NCT02169869

Conditions

1. Contraception

Interventions

1. Device: Mirena
2. Device: Paragard

Comparison of the proportion of women randomized to placement of IUD within 60 minutes of placental delivery or at their 6-week routine postpartum visit who report having an IUD in place at 3 months after delivery.. Inclusion Criteria: - Female - 18 yo or older - Singleton pregnancy at ≥32 weeks gestation at time of enrollment - Voluntarily requesting either copper T380A or levonorgestrel IUD (LNG-IUS) placement for postpartum contraception - English or Spanish speaking - Able to give consent and agree to the terms of the study - Less than 10 prenatal visits or 2 or more no show visits - Since IUDs are not on our hospital formulary, the patient must qualify for a Long Acting Reversible Contraceptive (LARC) IUD (this includes all Oregon Health Plan (OHP) or Citizen/Alien Waived Emergent Medical (CAWEM) insured patients or women with income <300% of the federal poverty line). --- T380A ---

Exclusion Criteria: - Anatomic uterine abnormalities that prevent proper fundal placement of IUD (obstructive myomata, bicornuate, septate, etc) - Chorioamnionitis (also consider other risk factors such as prolonged rupture of membranes >18 hours, prolonged labor >24 hours, fever >38C) - Puerperal sepsis - Unresolved postpartum hemorrhage - Extensive genital trauma - Current incarceration - Known or suspected untreated endocervical gonorrhea, chlamydia - Wilson's disease, copper allergy (Paragard only) - Known or suspected cervical or endometrial cancer or pelvic tuberculosis - Current breast cancer (LNG-IUS only) - Systemic lupus erythematosus (SLE) with severe thrombocytopenia (Paragard only) - Trophoblastic disease (benign or malignant) - AIDS not stable on antiretroviral Inclusion Criteria: - Female - 18 yo or older - Singleton pregnancy at ≥32 weeks gestation at time of enrollment - Voluntarily requesting either copper T380A or levonorgestrel IUD (LNG-IUS) placement for postpartum contraception - English or Spanish speaking - Able to give consent and agree to the terms of the study - Less than 10 prenatal visits or 2 or more no show visits - Since IUDs are not on our hospital formulary, the patient must qualify for a Long Acting Reversible Contraceptive (LARC) IUD (this includes all Oregon Health Plan (OHP) or Citizen/Alien Waived Emergent Medical (CAWEM) insured patients or women with income <300% of the federal poverty line). --- T380A ---

The novel SCu300A IUB™ (hereafter IUB™) will be evaluated for safety and effectiveness in comparison with a market approved standard T shaped IUD containing 380sq.mm. of copper. The Primary Endpoints for comparison are based on the objective and subjective parameters. The objective parameters are pregnancy rate, perforation, expulsion and mal -position rates, changes in the endometrial thickness, rate of complications such as infection and anemia and discontinuation rates after 2 years. The subjective parameters including Quality of Life (QoL) are: pain during insertion, menstrual characteristics and pain, bleeding in correlation to the bleeding pattern prior to insertion. The Secondary Endpoints are physician opinion (ease of use in insertion and removal) and subject satisfaction.

NCT02036177

Conditions

1. To Assess the Safety, Effectiveness and User Experience of the Scu 300A IUB

Interventions

1. Device: SCu300A IUB intrauterine device
2. Device: T380A IUD

Multivariate Assessment of the IUB Intrauterine Device Compared With a T380A IUD The novel SCu300A IUB™ (hereafter IUB™) will be evaluated for safety and effectiveness in comparison with a market approved standard T shaped IUD containing 380sq.mm. of copper. --- T380A ---

Many oral analgesic drugs such as the nonsteroidal anti-inflammatory drug (NSAID) are used to relieve pain from gynaecological procedures and dysmenorrhea. Hyoscine-N-butyl bromide, an antispasmodic drug is commonly used for relief of smooth muscle spasms and can be used to alleviate genito-urinary spasm. Some studies reported hyoscine couldn't relieve pain in minor gynaecological procedures. So the efficacy of Hyoscine-N-butyl bromide use is still controversial, and no previous studies investigated its effectiveness for pain relief in IUD insertion procedure.

NCT03499743

Conditions

1. IUD Insertion Pain

Interventions

1. Drug: hyoscine butyl bromide
2. Drug: Celecoxib 200mg
3. Drug: Placebo Oral Tablet

Celecoxib Versus Hyoscine Butyl-bromide in Reducing Pain Perception During Copper T380A Intrauterine Device Insertion: a Randomized Double-blind Controlled Trial. --- T380A ---

To investigate whether vaginal isonicotinic acid hydrazide administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications and pain in in Women Delivered Only by Cesarean Delivery.

NCT04499989

Conditions

1. IUCD Complication

Interventions

1. Drug: INH
2. Drug: Placebo Comparator

Clinical Outcomes of Vaginal Isonicotinic Acid Hydrazide (INH) Administration Prior to T380A Intrauterine Device Insertion in Women Delivered Only by Cesarean Delivery: a Randomized Double Blinded Clinical Trial. --- T380A ---

Vaginal Isonicotinic Acid Hydrazide (INH) Administration Prior to T380A Intrauterine Device Insertion To investigate whether vaginal isonicotinic acid hydrazide administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications and pain in in Women Delivered Only by Cesarean Delivery. --- T380A ---

This was a randomized controlled trial of 400 women who attended the outpatient clinic of Menoufia University Hospital for copper IUD insertion. The women were randomly assigned to cough and control groups.The primary outcome measure was the level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS).

NCT04602897

Conditions

1. Pain

Interventions

1. Other: forced coughing

MeSH:Cough

HPO:Cough

The primary outcome measure was the level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS).. Inclusion Criteria: - Non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---

A statistician not directly involved in the study prepared a computer generated randomization list and placed the allocation information in sequentially numbered sealed envelopes that were opened according to the attendance of the subjects after signing the informed consent Inclusion Criteria: - Non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---

We recruited non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---

The purpose of this study is to see if women presenting for emergency contraception (EC) are willing to accept the copper intrauterine device (IUD). This study will also compare the use of effective methods of contraception between women who selected the copper IUD or Plan B 6 months after they received EC.

NCT00669396

Conditions

1. Pregnancy

Interventions

1. Drug: Copper T380 IUD
2. Drug: levonorgestrel

MeSH:Emergencies

A Pilot Study of Copper T380A IUDs Versus Oral Levonorgestrel for Emergency Contraception. --- T380A ---

After medication abortion, women may quickly become pregnant again and therefore need an effective birth control method right away. Intrauterine devices (IUDs) are very effective for preventing pregnancy. IUDs are usually placed more than a month after abortion. This study will randomly assign women having a medication abortion to two groups, either having the IUD inserted one week after medication abortion or having the IUD inserted more than four weeks later. Women will be followed for six months to compare how many return for IUD placement in the two groups, how many are using the IUD after six months, experience with pain, bleeding, and cramping, how easy or difficult it is to insert the IUD, how many IUDs are expelled or removed, and how many women are using any birth control six months after the abortion.

NCT00737178

Conditions

1. Contraception

Interventions

1. Device: CuT380A

A Randomized Trial of Immediate Versus Delayed Insertion of the Copper T380A Following Medication Abortion. --- T380A ---

The purpose of this non-blinded randomized clinical trial is to pilot the design of a randomized clinical trial to be conducted in Malawi to investigate immediate postpartum insertion of the Copper T380 intrauterine contraceptive device (CuT380A-IUCD) compared to placement at the 6-week postpartum visit. The investigators hypothesize that it will be feasible to enroll 140 women into this study, and that women will find the 10 minute to 48 hour time frame for IUCD placement acceptable.

NCT01175161

Conditions

1. Contraception
2. Intrauterine Devices
3. Pilot Study
4. Africa

Interventions

1. Device: Copper T380A Intrauterine Device

A Pilot Study Of A Randomized Trial Comparing Two Different Time Frames For Copper T380A Intrauterine Contraception Insertion; Immediately Postpartum Compared To 4-6 Weeks Postpartum In Lilongwe, Malawi. --- T380A ---