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Recruiting NCT07736963

Discontinuation Recommendations for GLP-1 Receptor Agonists Prior to Colonoscopy: A Randomized Controlled Trial in Taiwan.

Conditions: GLP-1

Sex: All
Ages: 18 Years – 90 Years
Healthy volunteers: No
Phase: NA
Enrollment: 240
Sponsor: Fu Jen Catholic University Hospital

Location: FJUH New Taipei Taiwan

Summary

This study aims to evaluate the impact of different discontinuation intervals of GLP-1 receptor agonists prior to colonoscopy on bowel preparation quality and the need for repeat colonoscopy, in order to establish appropriate discontinuation recommendations.

Eligibility Criteria

Inclusion Criteria: * Inclusion Criteria for non GLP-1 user: * Individuals who are scheduled to undergo total colonoscopy for any reasons * Age between 18 to 70 years. * ECOG Performance status is 0 or 1. * Written consent to participate in the study has been obtained. * Outpatient department patient * Stop at least 3 days if current using medications that promote or inhibit gastrointestinal motility. Exclusion Criteria: * • Presence of severe comorbid conditions that preclude the safe performance of colonoscopy (e.g., unstable angina, recent myocardial infarction, decompensated heart failure, chronic respiratory disease, or bleeding diathesis). * History of prior gastric, small bowel, or colorectal segmental resection (patients with isolated appendectomy are eligible). * Family history of hereditary colorectal cancer syndromes. * Current or prior diagnosis of inflammatory bowel disease. * Known colorectal polyposis syndromes. * Any other condition deemed inappropriate for study participation at the discretion of the treating physician. * Body mass index (BMI) \> 40 kg/m². * Diagnosis of liver cirrhosis. * Diagnosis of Parkinson's disease. * Diagnosis of dementia. * Use of tricyclic antidepressants or opioid medications for more than 3 months.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07736963). StuddyBuddy aggregates publicly available trial information.