IRCT2013043013183N1CompletedPhase 2
Assessment of effect of Wild Mint product in Postprandial Distress Syndrome
shahed University of Medical Sciences0 sites100 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 65 years (—)
- Sex
- All
Inclusion Criteria
- •patients with 18-65 old years? Early Satiety? bothersome postprandial fullness? Without Organic Disorders on physical examination and Endoscopic
- •Exclusion criteria: Patients with organic disorders? The use of Chemicals and Herbals any other medication? History of Abdominal surgeries? History of bloody diarrhea? Pregnancy and lactation? Lack of interest in work? Not sign the consent
Exclusion Criteria
- Not provided
Investigators
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