Effect of Pimpinella Anise product in Postprandial Distress Syndrome
Phase 2
- Conditions
- Dyspepsia.Indigestion
- Registration Number
- IRCT2013101214980N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Inclusion Criteria: Patients within 18-65 years old with Postprandial Distress Syndrome.
Exclusion Criteria
Using of chemical and herbal drugs? History of abdominal surgeries? History of bloody diarrhea? Pregnancy and lactation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity Assessment of Dyspepsia. Timepoint: At baseline,at 2,4,12 weeks. Method of measurement: The Gastrointestinal Symptom Scale.;Quality of life. Timepoint: At Baseline? at 12 Weeks. Method of measurement: SF-36 Questionnaire.
- Secondary Outcome Measures
Name Time Method Side Effects. Timepoint: During the 12-week follow-up study. Method of measurement: Questionnaire.