Trials / Completed
CompletedNCT02037776
The Efficacy and Safety Study of Rikkunshito in Patients With Functional Dyspepsia
Double-blind Trial With Rikkunshito Versus Placebo on Efficacy and Safety in Patients With Functional Dyspepsia: Multi-center Study (DREAM Study)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 128 (actual)
- Sponsor
- Osaka City University · Academic / Other
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the efficacy and safety of Rikkunshito compared to placebo in Japanese subjects with Functional Dyspepsia (FD).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Rikkunshito | \- Oral administration of rikkunshito (2.5 g t.i.d) before meals for 8 weeks |
| DRUG | Rikkunshito placebo | \- Oral administration of rikkunshito placebo (2.5 g t.i.d) before meals for 8 weeks |
Timeline
- Start date
- 2014-04-03
- Primary completion
- 2016-03-25
- Completion
- 2016-03-25
- First posted
- 2014-01-16
- Last updated
- 2017-07-27
- Results posted
- 2017-07-27
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT02037776. Inclusion in this directory is not an endorsement.