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Clinical Trials/IRCT2013043013183N1
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

Sponsor
shahed University of Medical Sciences

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