Trial Details
COMPLETEDBasic Information
| Clinical ID | c4026 |
|---|---|
| Identifier | NCT01166789 |
| Trial Title | Lubiprostone Effects on Visceral Pain Sensitivity |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NO |
|---|---|
| Conditions | Irritable Bowel Syndrome |
| Interventions | DRUG: Lubiprostone|DRUG: Placebo |
Participant Information
| Sponsor | University of North Carolina, Chapel Hill |
|---|---|
| City | Chapel Hill |
| Country/Region | United States |
Enrollment Criteria
| Sex Requirement | ALL |
|---|---|
| Age Requirement | ADULT, OLDER_ADULT |
Study Design
| Study Type | INTERVENTIONAL |
|---|---|
| Phase | PHASE1 |
Time Information
| Start Date | 2008-02 |
|---|---|
| Primary Completion Date | 2010-08 |
| Completion Date | 2010-08 |