CTRI/2017/11/010529
Completed
Phase 4
Comparative Evaluation of Safety and Efficacy of Drotaverine Versus Mebeverine in Irritable Bowel Syndrome â?? A Randomized Double Blind Controlled Study. - Drotin DS/07/15
Walter Bushnell Pvt Ltd0 sites200 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Walter Bushnell Pvt Ltd
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients between 18 to 80 years of either gender
- •Fulfillment of IBS Rome III criteria
- •Written informed consent
Exclusion Criteria
- •Failure to meet all inclusion criteria
- •Pregnant females
- •Patients with comorbid diseases, coronary artery disease (CAD), chronic obstructive pulmonary disease (COPD), congestive heart failure (CHF)
- •Patients taking drugs which modify or aggravate symptoms (antidepressants, calcium channel blockers etc)
- •Patients having hypothyroidism \& gluten hypersensitivity
- •Any history of fever, passage of blood in stool, loss of weight, any organic disease of GI tract in the recent past
- •Patients on any other concomitant medication for abdominal pain, bowel disturbance or altering gastrointestinal motility
- •Malignancy of any other organ
Outcomes
Primary Outcomes
Not specified
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