Clinical trial
A Randomized, Double-blind, Placebo-controlled, Multicenter Phase III Clinical Trial, Efficacy and Safety Study of Changkang Granules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea ( Liver qi Affecting the Spleen Pattern)
NCT06753890 is registered in ClinicalTrials.gov with Tasly Pharmaceutical Group Co., Ltd as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized, Double-blind, Placebo-controlled, Multicenter Phase III Clinical Trial, Efficacy and Safety Study of Changkang Granules in the Treatment of Irritable Bowel Syndrome With Predominant Diarrhea ( Liver qi Affecting the Spleen Pattern)
- Lead sponsor
- Tasly Pharmaceutical Group Co., Ltd
- Phase
- Phase 3
- Overall status
- Not yet recruiting
- Start date
- December 30, 2024
- Completion date
- December 30, 2026
- Enrollment
- 520 (estimated)
- Sites
- 30
Conditions
As the registry lists them; a condition with its own page is linked.
diarrhea-predominant irritable boewl syndrome