Trial Details
COMPLETEDBasic Information
| Clinical ID | c3431 |
|---|---|
| Identifier | NCT02074579 |
| Trial Title | A Safety and Efficacy Study of Daikenchuto (TU-100) to Relieve Abdominal Bloating in Female Subjects With Irritable Bowel Syndrome |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Bowel Syndrome in Females |
| Interventions | DRUG: TU-100|DRUG: Placebo |
Participant Information
| Sponsor | Tsumura USA |
|---|---|
| City | Los Angeles |
| Country/Region | United States |
Enrollment Criteria
| Sex Requirement | FEMALE |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE2 |
Time Information
| Start Date | 2014-07 |
|---|---|
| Primary Completion Date | 2016-04 |
| Completion Date | 2016-04 |