Clinical Trial

Impact of Neuropathy on the Risk of Semaglutide-Induced Gastric Retention

Not Yet Recruiting
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Summary
A prospective, single-center, observational study to compare the risk of gastric retention between the exposure group (with neuropathy) and non-exposure group (without neuropathy) in diabetic patients receiving uninterrupted semaglutide therapy
Trial Details
NCT Number NCT07156591
Lead Sponsor Fudan University
Conditions Gastric Retention
Enrollment 460 participants
Start Date 2025-09-15
Primary Completion 2028-09-15 (estimated)
Study Completion 2028-09-15 (estimated)
Updated on ClinicalTrials.gov 2025-09-05