Trial Details
COMPLETEDBasic Information
| Clinical ID | c4098 |
|---|---|
| Identifier | NCT01056107 |
| Trial Title | Effects of ROSE-010 on GI Transit in Constipation Predominant Irritable Bowel Syndrome (C-IBS) Patients |
| Trial URL | Visit Original Page |
Study Information
| Study Results | YES |
|---|---|
| Conditions | Irritable Bowel Syndrome Constipation Predominant |
| Interventions | DRUG: ROSE-010|DRUG: Placebo |
Participant Information
| Sponsor | Mayo Clinic |
|---|---|
| City | Rochester |
| Country/Region | United States |
Enrollment Criteria
| Sex Requirement | FEMALE |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE1|PHASE2 |
Time Information
| Start Date | 2010-01 |
|---|---|
| Primary Completion Date | 2011-12 |
| Completion Date | 2011-12 |