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