Trials / Completed
CompletedNCT01316718
Mesalazine for the Treatment of Diarrhoea-predominant Irritable Bowel Syndrome (IBS-D)
Efficacy and Mode of Action of Mesalazine in the Treatment of Diarrhoea-predominant Irritable Bowel Syndrome (IBS-D).
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 108 (actual)
- Sponsor
- University of Nottingham · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the trial is to define the clinical benefit and possible mediators of the benefit of mesalazine in Irritable Bowel Syndrome (IBS) with diarrhoea. The investigators will therefore evaluate symptoms (primarily bowel frequency) and markers reflecting mast cell activation and small bowel tone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mesalazine | 2g oral granules, once a day for 1 week, then 2g oral granules, twice a day for 11 weeks |
| DRUG | Placebo | 2g oral granules, once a day for 1 week, then 2g oral granules, twice a day for 11 weeks |
Timeline
- Start date
- 2011-03-01
- Primary completion
- 2013-09-01
- Completion
- 2013-09-01
- First posted
- 2011-03-16
- Last updated
- 2014-01-17
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT01316718. Inclusion in this directory is not an endorsement.