Trials / Completed
CompletedNCT02260154
Effectiveness of Duspatalin® in Patients With Post-cholecystectomy Gastrointestinal Spasm
Effectiveness of Duspatalin® (Mebeverine Hydrochloride) 200 mg b.i.d. in Patients With Post-cholecystectomy Gastrointestinal Spasm: a Post Marketing Observational Program in the Russian Federation
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 220 (actual)
- Sponsor
- Abbott · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Prospective, multicenter, non-comparative, observational program designed to assess the effectiveness of a 2-6 weeks treatment with Duspatalin® 200mg bis in die = twice a day (BID) and changes in quality of life in patients with post-cholecystectomy gastro-intestinal spasms
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Mebeverine | Subjects treated by Duspatalin (mebeverine) 200 mg BID (bis in die = twice a day) upto 6 weeks in accordance with routine practice will be observed |
Timeline
- Start date
- 2015-07-01
- Primary completion
- 2016-10-01
- Completion
- 2016-10-01
- First posted
- 2014-10-09
- Last updated
- 2019-06-06
- Results posted
- 2019-06-06
Locations
21 sites across 1 country: Russia
Source: ClinicalTrials.gov record NCT02260154. Inclusion in this directory is not an endorsement.