Trials / Completed
CompletedNCT00987805
Efficacy of Banhasasim-tang on Functional Dyspepsia
Efficacy of Banhasasim-tang on Functional Dyspepsia : a Randomized, Double Blind, Placebo Controlled, Two-center Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 84 (actual)
- Sponsor
- Korea Health Industry Development Institute · Other Government
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess efficacy based on Gastrointestinal Symptom score and safety based on the rate of adverse event or laboratory findings of Banhasasim-tang administrated three times a day orally on functional dyspepsia.
Detailed description
Banhasasim-tang 1. Main 3 gram herb powder (including Rhizoma Pinelliae, Radix Scutellariae, Zingiberis Rhizoma, Panax ginseng, Glycyrrhiza uralensis Fisch, Zizyphi Fructus and Coptidis Rhizoma) of old oriental prescriptions for dyspepsia. 2. Usually having used for dyspepsia in asia 3. Need for correct clinical information by RCT
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Banhasasim-tang | Form : granules Contents : It consists of seven Herbs. It contains Rhizoma Pinelliae, Radix Scutellariae, Zingiberis Rhizoma, Panax ginseng, Glycyrrhiza uralensis Fisch, Zizyphi Fructus and Coptidis Rhizoma Dosage and frequency : 9g per day (three times a day) Route of administration : Oral Administration duration : 42 days in the study |
| DIETARY_SUPPLEMENT | Corn-starch granules | This placebo has the same form, color, and flavor as experimental intervention.The dosage, frequency and duration is also same as experimental intervention. |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2011-01-01
- Completion
- 2011-01-01
- First posted
- 2009-10-01
- Last updated
- 2012-06-21
Locations
2 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT00987805. Inclusion in this directory is not an endorsement.