Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTBanhasasim-tangForm : 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_SUPPLEMENTCorn-starch granulesThis 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.