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    HP:0003003: Colon cancer

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (9)


    Name (Synonyms) Correlation
    drug3614 Shared Decision Making Wiki 0.50
    drug2109 Late-Dexamethasone Wiki 0.50
    drug1345 Educational meetings and visual prompts Wiki 0.50
    Name (Synonyms) Correlation
    drug1344 Educational Program on Air Pollution as a Health Risk Reduction Strategy Wiki 0.50
    drug1473 Extracorporeal left hemicolectomy anastomosis Wiki 0.50
    drug1997 Intracorporeal left hemicolectomy anastomosis Wiki 0.50
    drug1332 Early-Dexamethasone Wiki 0.35
    drug895 Chemotherapy Wiki 0.35
    drug1336 Echocardiography Wiki 0.29

    Correlated MeSH Terms (1)


    Name (Synonyms) Correlation
    D003110 Colonic Neoplasms NIH 1.00

    Correlated HPO Terms (0)


    Name (Synonyms) Correlation

    Clinical Trials

    Navigate: Correlations   HPO

    There are 4 clinical trials


    1 Patients' Preferences About Rescheduling Colonoscopies Delayed Due to COVID-19: Cross Sectional Study

    The study is a cross-sectional survey study targeting patients aged 45-75 who had their screening or surveillance colonoscopy postponed or delayed due to the COVID pandemic. Study staff will survey a random subsample of patients to assess anxiety, COVID risk tolerance, cancer worry, willingness to screen and barriers to screening colonoscopy, and preference for colonoscopy and alternative colon cancer screening options. Eligible patients will be sent a survey packet in the mail that will include a cover letter, an information sheet describing the study, an incentive, and the survey. The cover letter will include information for participants to opt-out if they desire. Patients will be asked to complete the survey and return it back to study staff. Consent is implied with return of the survey. For the study, staff plan to invite 300 patients and expect to receive 195 completed surveys. Analyses will examine whether COVID-19 has changed patients' interest in colon cancer screening and the strength of patients' preferences for colonoscopy and other approaches to colon cancer screening. It will then examine factors associated with positive and negative views on rescheduling colonoscopies such as anxiety, worry, and risk perceptions.

    NCT04432870
    Conditions
    1. Colon Cancer
    MeSH:Colonic Neoplasms
    HPO:Colon cancer Neoplasm of the colon

    Primary Outcomes

    Description: Item with 5-point response assessing whether COVID-19 has increased, decreased or not changed interest in colon cancer screening

    Measure: Interest in colon cancer screening

    Time: at start of study--between one week and 2 months after start of study

    Secondary Outcomes

    Description: Item with 5-point response (definitely want to definitely do not want) measuring interest in having a stool test for colon cancer

    Measure: Preference for stool testing

    Time: at start of study--between one week and 2 months after start of study

    Description: Item with 5-point response (definitely want to definitely do not want) measuring interest in postponing colonoscopy for one year

    Measure: Preference for postponing colonoscopy for one year

    Time: at start of study--between one week and 2 months after start of study

    Description: Item with 5 point response (extremely worried to not at all worried) assessing worry about the delay of the colonoscopy on their colon cancer risk

    Measure: Worry about delay

    Time: at start of study--between one week and 2 months after start of study

    Description: Item with 5-point response (very high to very low) assessing patients' perception about risk of getting COVID-19 from having a colonoscopy

    Measure: Risk perception on COVID-19

    Time: at start of study--between one week and 2 months after start of study
    2 RESECTION AND INTRACORPOREAL ANASTOMOSIS IN LAPAROSCOPIC LEFT COLECTOMY AS AN ADAPTATION TO THE PANDEMIC CAUSED BY SARS-CoV-2 (COVID19). A COMPARATIVE COHORT STUDY

    OBJECTIVE: The aim of the study is to demonstrate that the intracorporeal resection and anastomosis in left-sided colon cancer, sigma and upper rectum, is not inferior to extracoprporeal resection and anastomosis, in terms of anastomotic leakage. BACKGROUND: Due to the recent events of a pandemic respiratory disease secondary to infection by SARS-CoV-2 virus or coronavirus 19 (COVID19), surgeons have been forced to adapt our surgical procedures in order to minimize exposure to the virus as much as possible. Based on the recommendations in case of surgery in patients with highly contagious viral diseases, the latest studies suggest minimally invasive accesses to minimize the risk of contagion. One of the proposed measures is the performance of intracorporeal anastomoses. Therefore, given the extensive experience of our center in minimally invasive surgery and studies on the validation of intracorporeal anastomosis techniques in both laparoscopic surgery of the right colon and rectum (TaTME), and the study of advantages that they can provide to the patient, our intention is to apply it to surgery on the left colon, sigma and upper rectum. Our hypothesis is that exteriorization of the colon through an accessory incision increases the risk of tension at the mesocolon level, thus increasing the risk of vascular deficit at the level of the staple area and it may increase the rate of anastomotic leakage. In this sense, studies that validate a standard technique of intracorporeal anastomosis in left colon surgery and that demonstrate its benefit with respect to extracorporeal anastomosis are lacking. We intend to describe a new intracorporeal anastomosis technique (ICA) that is feasible and safe for the patient and that can be applied universally. Once the ICA technique is established, it will allow us to determine its non-inferiority compared to the standard technique performed up to now with extracorporeal anastomosis. METHODS: All consecutive patients with left-sided, sigma and upper rectum adenocarcinoma will be included into a prospective cohort and treated by laparoscopy with totally intracorporeal resection and anastomosis. They will be compared with a retrospective cohort of consecutive patients of identical characteristics treated by laparoscopy with extracorporeal resection and anastomosis, in the immediate chronological period.

    NCT04456933
    Conditions
    1. Colon Cancer
    Interventions
    1. Procedure: Extracorporeal left hemicolectomy anastomosis
    2. Procedure: Intracorporeal left hemicolectomy anastomosis
    MeSH:Colonic Neoplasms
    HPO:Colon cancer Neoplasm of the colon

    Primary Outcomes

    Description: Percentage of anastomic leak (defined in accordance with Peel et al.).

    Measure: Percentage of anastomotic leak (AL)

    Time: 30 days

    Secondary Outcomes

    Description: Dindo-Clavien Classification

    Measure: Rate of global morbidity

    Time: 30 days

    Description: SSI in accordance with the Center for Disease Control (CDC) National

    Measure: Rate of Surgical site infection

    Time: 30 days

    Description: Percentage of re-interventions due to surgical complications

    Measure: Rate of Re-interventions

    Time: 30 days
    3 Improving Food Pleasure and Intake of Oncology Patients Receiving Chemotherapy

    The global cancer burden is estimated to have risen to 18.1 million new cases in 2018 (WHO), with a trend of ongoing growth. This very frequent illness exerts tremendous physical, emotional and financial strain on individuals, families, communities and health systems. Malnutrition (under- or over-nutrition) is highly prevalent in cancer patients receiving chemotherapy and is an important predictor of morbidity, mortality, treatment response and toxicity. Alterations in taste and smell are frequently reported as side effect of chemotherapy and may contribute strongly to malnutrition and to a worsen quality of life and wellbeing social, emotional, and role functioning. There are evidences that chemotherapy influences food liking and appetite with implications for food behaviours, including food enjoyment, food preference and dietary intake. A linkage between alterations in taste and /or smell and food behaviours has been reported by some studies but not all, suggesting that there is a need for more research using common standardised methodologies and larger sample size to gain a further insight into this topic.

    NCT04495387
    Conditions
    1. Colon Cancer
    2. Breast Cancer
    3. Chemotherapeutic Toxicity
    Interventions
    1. Drug: Chemotherapy
    MeSH:Colonic Neoplasms
    HPO:Colon cancer Neoplasm of the colon

    Primary Outcomes

    Description: To better understand alteration of taste/smell and food behaviours by the self-report responses, using an adapted version of a questionnaire set up to measure taste changes due to COVID-19

    Measure: change of taste chemotherapy-related alterations

    Time: the variables will be measured at four time points: before chemotherapy (T0), after 4 cycles (T1, each cycle is 21 days), at the end of chemotherapy (T2, 6 months from T0) and three months after the conclusion of the therapy (T3, 9 months from T0)

    Secondary Outcomes

    Description: Emotions elicited by foods will be measured on a selection of foods through an EmoSemio questionnaire, a self-report measure of emotion developed based on preliminary interviews

    Measure: Emotions elicited by foods

    Time: the variables will be measured at four time points: before chemotherapy (T0), after 4 cycles (T1, each cycle is 21 days), at the end of chemotherapy (T2, 6 months from T0) and three months after the conclusion of the therapy (T3, 9 months from T0)
    4 Engaging Patients in Colon Cancer Screening Decisions During COVID-19

    The goal of the study is to examine whether a shared decision making intervention improves decision making about colon cancer screening for patients who had their colonoscopy delayed or postponed due to the COVID pandemic. Eligible patients (n=800) will be randomly assigned to either the intervention or control arm. A subset will be surveyed about 6 weeks post intervention to measure shared decision making, their intention to follow through with screening, and their decisional conflict. Study staff will conduct medical chart review to track receipt of colon cancer screening within 6 months. The statistician will test whether patients in the intervention arm report more shared decision making, less decisional conflict, higher intention to follow through on screening and have higher screening rates compared to those in the control arm.

    NCT04548531
    Conditions
    1. Colon Cancer
    Interventions
    1. Behavioral: Shared Decision Making
    MeSH:Colonic Neoplasms
    HPO:Colon cancer Neoplasm of the colon

    Primary Outcomes

    Description: short patient reported scale asks patients about discussion of options, pros and cons of colonoscopy and discussion of patients' preferences. Total scores range from 0-4 with higher scores indicating higher shared decision making.

    Measure: Shared Decision Making (SDM) Process Scale Score

    Time: 6 weeks after intervention

    Secondary Outcomes

    Description: the 4-item version of the decisional conflict scale, total score ranges from 0-4 with greater scores indicating less decisional conflict.

    Measure: Decisional Conflict (SURE scale)

    Time: 6 weeks after intervention

    Description: One item will assess patients' preferred approach to screening (with responses of colonoscopy, stool card test, no screening, not sure).

    Measure: Patient's preferred approach to screening

    Time: 6 weeks after intervention

    Description: One item will assess patients' intention to follow through with their preferred approach on a 5-point scale from not at all likely to extremely likely.

    Measure: Intention to screen

    Time: 6 weeks after intervention

    Description: Percentage of patients who had completed colon cancer screening test

    Measure: Colon cancer screening rate

    Time: 6 months after randomization

    HPO Nodes


    Reports

    Data processed on September 26, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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