Clinical Trial

Acotiamide vs Itopride in Postprandial Distress Syndrome

Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The goal of this study is to "To compare the efficacy and safety of Acotiamide versus Itopride in patient with post prandial distress syndrome type of functional dyspepsia"
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-09-12.
Trial Details
NCT Number NCT07174297
Lead Sponsor Getz Pharma
Collaborators: Rawalpindi Medical College, Pakistan
Conditions Postprandial Distress Syndrome
Enrollment 152 participants
Start Date 2025-10-30
Primary Completion 2026-12-30 (estimated)
Study Completion 2027-04-30 (estimated)
Updated on ClinicalTrials.gov 2025-09-23