Clinical trial
Impact of a One-Week Discontinuation of Semaglutide on Gastric Retention and Endoscopic Mucosal Visibility Scores
Opening soon · Not applicable · 1 countries · Registry ID NCT07152756
Opening soonNot applicableObservational
What this study is about
A prospective, single-center, observational study to compare the risk of gastric retention and endoscopic mucosal visibility between the exposure group (one-week discontinuation of semaglutide before EGD) and non-exposure group (no semaglutide use before EGD)
A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.
Basic eligibility
Age18 Years to Not listed
SexAll
Healthy volunteersNot accepted
ConditionGastric Retention
Full registry criteria
Inclusion Criteria 1. Subjects who have either: (i) been on long-term semaglutide therapy (≥4 weeks, any dosage) and discontinued use for one week prior to gastroscopy (with the last dose 8-14 days before the procedure), or(ii) never used semaglutide. 2. For patients with diabetes mellitus (DM), HbA1c \< 9% to ensure adequate glycemic control. 3. Age ≥ 18 years, with no restriction on sex. 4. American Society of Anesthesiologists (ASA) physical status classification I-II. 5. Fasting for at least 8 hours and no water intake for at least 4 hours before gastroscopy. 6. Undergoing painless (sedated) endoscopy. Exclusion Criteria 1. History of hiatal hernia or any previous gastric surgery (including gastrectomy, Roux-en-Y gastric bypass, etc.). 2. Pregnancy. 3. Medically unfit for gastrointestinal endoscopy. 4. Deemed unsuitable for participation at the discretion of the investigators.
Treatments and study arms
Esophagogastroduodenoscopy
Procedure
Assess the gastric retention and the endoscopic mucosal visibility score during esophagogastroduodenoscopy
Primary outcomes
Rate of gastric retentionimmediately after the esophagogastroduodenoscopy
Gastric retention was defined as the presence of solid residues in the stomach or liquid retention exceeding 1.5 mL/kg
Study locations
1 locations were listed when this page was built. The first 40 are shown.
Huadong hospital, Fudan university🇨🇳 Shanghai, Shanghai Municipality, China