CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


DoxycyclineWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (10)


Name (Synonyms) Correlation
drug2921 non interventional Wiki 0.50
drug881 Exercise Group Wiki 0.50
drug2719 Zinc Sulfate Wiki 0.50
drug1919 Prone Positioning (PP) Wiki 0.50
drug2977 questionnaire assesment Wiki 0.22
drug560 Chloroquine Wiki 0.18
drug1270 Ivermectin Wiki 0.12
drug262 Azithromycin Wiki 0.08
drug1822 Placebo Wiki 0.06
drug1086 Hydroxychloroquine Wiki 0.05

Correlated MeSH Terms (10)


Name (Synonyms) Correlation
D010146 Pain NIH 0.50
D001416 Back Pain NIH 0.50
D017116 Low Back Pain NIH 0.50
D059350 Chronic Pain NIH 0.41
D013577 Syndrome NIH 0.06
D055371 Acute Lung Injury NIH 0.05
D012127 Respiratory Distress Syndrome, Newborn NIH 0.05
D012128 Respiratory Distress Syndrome, Adult NIH 0.04
D045169 Severe Acute Respiratory Syndrome NIH 0.03
D018352 Coronavirus Infections NIH 0.02

Correlated HPO Terms (4)


Name (Synonyms) Correlation
HP:0003418 Back pain HPO 0.50
HP:0012531 Pain HPO 0.50
HP:0003419 Low back pain HPO 0.50
HP:0012532 Chronic pain HPO 0.41

There are 4 clinical trials

Clinical Trials


1 A Randomized Study Evaluating the Safety and Efficacy of Hydroxychloroquine and Zinc in Combination With Either Azithromycin or Doxycycline for the Treatment of COVID-19 in the Outpatient Setting

This is a randomized, open-label trial to assess the safety and efficacy of hydroxychloroquine, and zinc in combination with either azithromycin or doxycycline in a higher risk COVID-19 positive outpatient population.

NCT04370782 COVID-19 Drug: Hydroxychloroquine Drug: Azithromycin Drug: Zinc Sulfate Drug: Doxycycline

Primary Outcomes

Description: Patients will be assessed on day 5 for when COVID-19 symptoms completely resolve compared to baseline (day 1 of trial)

Measure: Time to Resolution of Symptoms relative to baseline (day 1 of trial)

Time: Day 5

Description: Patients will be assessed on day 14 for when COVID-19 symptoms completely resolve compared to baseline (day 1 of trial)

Measure: Time to Resolution of Symptoms relative to baseline (day 1 of trial)

Time: Day 14

Description: Patients will be assessed on day 21 for when COVID-19 symptoms completely resolve compared to baseline (day 1 of trial)

Measure: Time to Resolution of Symptoms relative to baseline (day 1 of trial)

Time: Day 21

Description: Number of participants hospitalized and/or requiring repeat ER visits related to COVID-19 complications

Measure: Number of participants hospitalized and/or requiring repeat ER visits

Time: 21 days

Description: If hospitalized, number of participants admitted to the ICU, and number of days in the ICU

Measure: ICU Length of Stay

Time: Until Discharged up to 30 days

Description: If placed on ventilator, number of days on a ventilator

Measure: Ventilator

Time: Until extubated up to 30 days

Secondary Outcomes

Description: Severity of symptoms evaluated at day 5, day 14, and day 21 scored by the participant for feverishness, sore throat, cough, shortness of breath, myalgias. (0 =none; 1 = mild; 2 = moderate; 3 = severe)

Measure: Severity of symptoms

Time: Day 5, Day 14, and Day 21

Description: Number of participants with adverse events due to drug regimen

Measure: Number of participants with adverse events due to drug regimen

Time: 21 days

Description: Assess all patients to evaluate for QTc prolongation >500ms

Measure: Number of participants with QTc prolongation >500ms

Time: Days 1 thru 5, Day 10, Day 21

2 Doxycycline Versus Placebo in COVID-19 + Patients Without Hospitalization Criteria: Prospective, Multicenter, Randomized, Double-blind Study

The aim of the study is to compare a treatment with doxycycline vs a placebo as soon as the patient is confirmed COVID-19 + and before the onset of oxygen dependence with the aim of reducing or even abolishing the cytokine explosion and thus the evolution towards a serious form of the disease which can lead to death. Three criteria support the rational use of tetrcycline in COVI-19 (1) The coronaviruses is known to bind to metalloproteases (MMPs) of the host, in particular to ensure viral survival. Tetracyclines are known to chelate zinc from MMPs. Their chelating activity may help inhibit COVID19 infection by limiting its ability to replicate in the host. (2) Tetracyclines may also be able to inhibit the replication of positive-polarity single-stranded RNA viruses, such as COVID19 (demonstrated on the dengue virus). (3) In addition, tetracyclines are modulators of innate immunity (anti-inflammatory activity), a property used in the treatment of inflammatory skin diseases for many years. These modulating effects are noted on several targets of innate immunity: They can decrease the expression of NFKB, the release of inflammatory cytokines such as TNF-α, IL-1β and IL-6, inhibit granulomas inflammatory and free radical release. Tetracyclines could therefore participate in limiting the cytokine release induced by COVID19. Their lipophilic nature and their strong pulmonary penetration could allow them to inhibit viral replication.

NCT04371952 COVID19 Drug: Doxycycline Drug: Placebo

Primary Outcomes

Description: Percentage of patients with clinical worsening (SaO2 ≤ 93%) after at least 48 hours of treatment

Measure: Percentage of Patients with Clinical Respiratory Aggravation

Time: after at least 48 hours of treatment

Description: Percentage of patients hospitalized after at least 48 hours of experimental treatment

Measure: Percentage of patients hospitalized

Time: after at least 48 hours of experimental treatment

Description: Percentage of patients requiring ventilatory assistance

Measure: Percentage of patients requiring ventilatory assistance

Time: Day 0 to Day 28

Secondary Outcomes

Description: Number of positive SARS-CoV-2 PCR tests on D-1 / D0 and D7 (+/- 2 days)

Measure: Positive SARS-CoV-2 PCR Test

Time: Day -1 or day 0 AND Day 7

Description: Duration of symptoms (fever, painful symptoms: headache, sore throat, dyspnea)

Measure: Duration of symptoms

Time: Day 0 to Day 28

Description: Total duration of hospitalization

Measure: Duration of hospitalization

Time: From day 0 until to the end of hospitalization or date of death for any cause, whichever came first, assessed up to 3 months after Day0

Description: Duration of hospitalization in intensive care or reanimation

Measure: Hospitalization intensive care or reanimation

Time: From day 0 until to the end of hospitalization or date of death for any cause, whichever came first, assessed up to 3 months after Day0

Description: Duration of mechanical ventilatory assistance

Measure: Duration of mechanical ventilatory assistance

Time: to the end of mechanical ventilatory assistance if any, assessed up to 3 months after Day0

Description: Percentage of deaths related to SARS-CoV-2 infection

Measure: Percentage of deaths related to SARS-CoV-2

Time: Day 28, or end of hospitalization if any (assessed up to 3 months after Day0)

Description: Number of AE / SAE in both arms

Measure: AE / SAE in both arms

Time: Day 28, or end of hospitalization if any (assessed up to 3 months after Day0)

3 The Efficacy of Ivermectin and Doxycycline in COVID-19 Treatment

Efficacy of Ivermectin and Doxycycline in COVID-19 treatment

NCT04403555 COVID Drug: Ivermectin Drug: Doxycycline Drug: Chloroquine

Primary Outcomes

Description: The number of patients with improvement or mortality

Measure: The number of patients with improvement or mortality

Time: 1 month

4 RepurpoSing Old Drugs TO SuppRess a Modern Threat: The STORM Trial

The primary aim of this study is to test whether Doxycycline can benefit patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections by inhibiting the replication of the virus while at the same time blocking the development of cytokine storms or inhibiting cytokine-associated coagulopathy respectively. The investigators hypothesize that Doxycycline will will improve survival and reduce morbidity in SARS-CoV-2 infected patients. A secondary aim is to identify genetic variants that predict either an unusually mild disease or an unusually severe disease - knowledge that can be used to design new and precise medications and to be able to predict patients who might get into early trouble and to therefore hospitalize them.

NCT04433078 Cytokine Storm SARS-CoV-2 Drug: Doxycycline Drug: Placebo

Primary Outcomes

Description: Days Alive and Out of Hospital (Composite Endpoint)

Measure: Time Free of Either Hospitalization, Hypoxemia, ICU Admission or Death

Time: 21 days

Secondary Outcomes

Description: Change From Baseline of Nasopharyngeal Luminex NxTAG CoV (Positive/Negative)

Measure: NP SARS-CoV-2 PCR

Time: 21 days

Description: Change From Baseline of SARS-CoV-2 Serum Quantitative Viral Load

Measure: SARS-CoV-2 Serum Quantitative Viral Load

Time: 21 days

Description: Change From Baseline of SARS-CoV-2 IgM/IgG Antibodies (Positive/Negative)

Measure: SARS-CoV-2 IgM/IgG Antibodies

Time: 21 days

Description: Change From Baseline of White Blood Count (CBC) K/mm3

Measure: White Blood Cell Count (WBC)

Time: 21 days

Description: Change From Baseline of Absolute Lymphocyte Count (ALC) K/mm3

Measure: Absolute Lymphocyte Count (ALC)

Time: 21 days

Description: Change From Baseline of C-Reactive Protein (CRP) mg/dL

Measure: C-Reactive Protein (CRP)

Time: 21 days

Description: Change From Baseline of N-Terminal Pro-B-Type Natriuretic Peptide (Pro-BNP) pg/mL

Measure: N-Terminal Pro-B-Type Natriuretic Peptide (Pro-BNP)

Time: 21 days

Description: Change From Baseline of High Sensitivity Troponin I (hsTnT) ng/mL

Measure: High Sensitivity Troponin I (hsTnT)

Time: 21 days

Description: Change From Baseline of Tumor Necrosis Factor Alpha (TNF-a)

Measure: Tumor Necrosis Factor Alpha (TNF-a)

Time: 21 days

Description: Change From Baseline of IL-1

Measure: IL-1

Time: 21 days

Description: Change From Baseline of IL-1B

Measure: IL-1B

Time: 21 days

Description: Change From Baseline of IL-6

Measure: IL-6

Time: 21 days


No related HPO nodes (Using clinical trials)