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Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

4 clinical studies listed.

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Gastric Retention

Tundra lists 4 Gastric Retention clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07251803

GLP1 Fasting Status and Gastric Retention Using Gastric Ultrasound

This study will enroll patients 18 years and older who are taking a GLP-1/GIP medication and 1) are scheduled for elective surgery and meet ASA fasting guidelines (nothing by mouth for at least 8 hours prior), or 2) scheduled elective colonoscopy and have been on a clear liquid diet for at least 24 hours prior. Participants will have a gastric ultrasound prior to surgery to measure any retained gastric contents. The purpose of this study is to determine if people taking GLP-1 receptor agonists and who fast normally are at an equal risk for having retained gastric contents after appropriately fasting for surgery, compared to patients who are on a liquid only diet for 24 hours prior to surgery.

Gender: All

Ages: 18 Years - Any

Updated: 2026-02-25

1 state

Gastric Retention
NOT YET RECRUITING

NCT07276763

Impact of Discontinuing GLP-1 Receptor Agonists for Two Weeks Prior to Upper Endoscopy on the Risk of Gastric Retention

A retrospective observational study to explore the impact of discontinuing GLP-1 receptor agonists for two weeks prior to upper endoscopy on the risk of gastric retention

Gender: All

Updated: 2025-12-11

1 state

Gastric Retention
NOT YET RECRUITING

NCT07156591

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

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

Gender: All

Ages: 18 Years - Any

Updated: 2025-09-05

1 state

Gastric Retention
NOT YET RECRUITING

NCT07152756

Impact of a One-Week Discontinuation of Semaglutide on Gastric Retention and Endoscopic Mucosal Visibility Scores

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)

Gender: All

Ages: 18 Years - Any

Updated: 2025-09-03

1 state

Gastric Retention