Clinical Trial

Vonoprazan Alone vs With Itopride for Functional Dyspepsia: The VIVA Trial

Recruiting
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Summary
The VIVA trial is a 12-week, randomized, interventional study comparing vonoprazan monotherapy versus vonoprazan plus itopride combination therapy in adults with functional dyspepsia (FD). FD is a common digestive disorder causing upper stomach discomfort, fullness after meals, and early satiety. The study aims to determine if adding itopride, a prokinetic that improves stomach emptying, to vonoprazan, a strong acid-suppressing drug, provides better symptom relief than vonoprazan alone. Participants will be randomly assigned to receive either treatment, and their symptoms, quality of life, and safety outcomes will be monitored throughout the study. The trial will help guide the best management strategy for FD by targeting both acid-related and motility-related symptoms.
Trial Details
NCT Number NCT07731542
Lead Sponsor Asian Institute of Gastroenterology, India
Conditions Functioanl Dyspepsia
Enrollment 192 participants
Start Date 2026-01-10
Primary Completion 2027-01-10 (estimated)
Study Completion 2027-02-10 (estimated)
Updated on ClinicalTrials.gov 2026-07-28