Trials / Completed
CompletedNCT02460601
The Efficacy and Safety of Qizhiweitong Granule on Patients With Functional Dyspepsia in a Multi-center Clinical Study
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 400 (actual)
- Sponsor
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The study aims to verify the efficacy and safety of Qizhiweitong granule on Chinese patients with functional dyspepsia diagnosed by the Rome III criteria. It includes two subtypes of functional dyspepsia, postprandial distress syndrome or abdominal pain syndrome.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Qizhiweitong granule |
Timeline
- Start date
- 2013-12-01
- Primary completion
- 2015-08-01
- Completion
- 2015-10-01
- First posted
- 2015-06-02
- Last updated
- 2015-12-09
Source: ClinicalTrials.gov record NCT02460601. Inclusion in this directory is not an endorsement.