Clinical Trials Directory

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

TypeNameDescription
DRUGMebeverineSubjects 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.