Trial Details
TERMINATEDBasic Information
| Clinical ID | c3897 |
|---|---|
| Identifier | NCT01358708 |
| Trial Title | Treatment of Diarrhea-predominant Irritable Bowel Syndrome (IBS-D) With LACTEOL® 340 mg |
| Trial URL | Visit Original Page |
Study Information
| Study Results | YES |
|---|---|
| Conditions | Diarrhea-predominant Irritable Bowel Syndrome |
| Interventions | DRUG: LACTEOL® 340 mg|DRUG: PLACEBO |
Participant Information
| Sponsor | Forest Laboratories |
|---|---|
| City | Bordeaux |
| Country/Region | France |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE3 |
Time Information
| Start Date | 2010-06 |
|---|---|
| Primary Completion Date | 2011-09 |
| Completion Date | 2011-09 |