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The effect of mesalazine and nortriptyline in patients with irritable bowel syndrome with diarrhea: A randomized clinical trail

Phase 3
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
Inclusion Criteria

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.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
Bloating. Timepoint: prior to intervention and 8 weeks after intervention. Method of measurement: IBS, Adequate Relief (IBS, AR).
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