The effect of mesalazine and nortriptyline in patients with irritable bowel syndrome with diarrhea: A randomized clinical trail
- Conditions
- irritable bowel syndrome.Irritable bowel syndrome with diarrhoea
- Registration Number
- IRCT201506171647N4
- Lead Sponsor
- Vice Chancellor for research; Shahroud University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
presence of clinical findings of diarrhea predominant irritable bowel syndrome according to ROME III criteria.
Exclusion criteria: use of analgesic drugs; pregnant women; breast feeding; patients with major depressive disorder (MDD) according to DSM-IV-TR; gastrointestinal bleeding; presence of any finding in favor of organic disorders in the lab tests; or organic disorder in colonoscopy of high risk patients; history of malignancy; use of illicit drugs; patients with constipation and mixed predominant irritable bowel syndrome.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity abdominal pain. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: Questionnaire (IBS, Symptom Severity Scoring) and visual scale of pain.;Frequency of abdominal pain. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: Questionnaire (IBS, Symptom Severity Scoring).;Dissatisfaction with bowel habits. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: Questionnaire (IBS, Symptom Severity Scoring) and visual scale of pain.;Interference with quality of life. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: Questionnaire (IBS, Symptom Severity Scoring).;Frequency of bowel habit. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: Questionnaire (IBS, Symptom Severity Scoring).
- Secondary Outcome Measures
Name Time Method Bloating. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: IBS, Adequate Relief (IBS, AR).