Trial Details
COMPLETEDBasic Information
| Clinical ID | c4720 |
|---|---|
| Identifier | NCT00067457 |
| Trial Title | Study In Women With Severe Diarrhea-Predominant Irritable Bowel Syndrome Having Failed Conventional Therapy |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Colon|Irritable Bowel Syndrome (IBS) |
| Interventions | DRUG: alosetron |
Participant Information
| Sponsor | GlaxoSmithKline |
|---|---|
| City | Birmingham |
| Country/Region | United States |
Enrollment Criteria
| Sex Requirement | FEMALE |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE3 |
Time Information
| Start Date | 2003-06 |
|---|---|
| Primary Completion Date | 2005-12 |
| Completion Date | 2005-12 |