Trial Details
RECRUITINGBasic Information
| Clinical ID | c672 |
|---|---|
| Identifier | NCT06247046 |
| Trial Title | A Study to Evaluate the Efficacy and Safety of Live SK08 Powder in Patients With IBS-D |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Bowel Syndrome With Diarrhea |
| Interventions | DRUG: Live SK08 powder|DRUG: Placebo |
Participant Information
| Sponsor | Guangzhou Zhiyi Biotechnology Co., Ltd. |
|---|---|
| City | Wuxi |
| Country/Region | China |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE3 |
Time Information
| Start Date | 2024-03-16 |
|---|---|
| Primary Completion Date | 2026-04 |
| Completion Date | 2027-01 |