drugset / Trial / NCT05199441
Efficacy of Galeo® in Patients With Postprandial Distress Syndrome Subtype in Functional Dyspepsia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | dihydroxydibutylether | Unknown | 1500 mg | — |