drugset / Trial / NCT05199441

Efficacy of Galeo® in Patients With Postprandial Distress Syndrome Subtype in Functional Dyspepsia

NCT05199441 ↗

Phase 4 Completed 226 enrolled Pusan National University Yangsan Hospital
RandomizedParallel-groupTriple-blindTreatment

Summary

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Galeo® on dyspepsia symptoms in patients with postprandial distress syndrome subtype in functional dyspepsia for 8 weeks.

Timeline

Start
2022-02-25
Primary completion
2023-07-05
Completion
2023-07-07

Drugs

EvaluationDrugModalityDoseRoute
Subject dihydroxydibutylether Unknown 1500 mg —

Indications