Mayo Clinic registers Phase 4 tirzepatide reflux and gastric physiology study
The crossover-style comparison against saline placebo uses 96-hour wireless pH recording starting about 48 hours after dosing.
PR
By Priya Raman · Science Reporter
Oct 26 08:00 ETSource: ClinicalTrials.gov
The wire
- 01ClinicalTrials.gov entry NCT07893457 will test whether a single 7.5 mg subcutaneous dose of tirzepatide increases total esophageal acid exposure time versus saline placebo in adults with obesity.
- 02Reflux and delayed gastric emptying are recurring clinical questions for incretin prescribers, and this study targets esophagogastric junction mechanics directly rather than relying on symptom reports.
- 03The trial is listed as not yet recruiting with a start date of October 26, 2026, and it examines a single acute dose, not chronic therapy.
From the source
Read at clinicaltrials.govEffects of Tirzepatide on Esophagogastric Junction Mechanics, Reflux Burden, and Gastric Physiology in Adults With Obesity
NCT07893457 · PHASE4 · NOT YET RECRUITING · Sponsor: Mayo Clinic · Conditions: Obese Adults.
Source URL https://clinicaltrials.gov/study/NCT07893457
