The effect of Specific Dietary Interventions in Postprandial Distress Syndrom
Not Applicable
- Conditions
- Functional dyspepsia.Indigestion
- Registration Number
- IRCT2015050322049N1
- Lead Sponsor
- Shahed University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients with 18-75 years old;
Willing to cooperate;
Early Satiety or bothersome postprandial fullness more than 3 months;
Without Organic Disorders on physical examination;
normal Endoscopic.
Exclusion Criteria
Patients with organic disorders; T
he use of Chemicals and Herbals any other medication;
History of Abdominal surgeries;
History of bloody diarrhea;
Pregnancy and breast feeding;
Lack of interest in work;
Not sign the consent.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity Assessment of Dyspepsia. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.
- Secondary Outcome Measures
Name Time Method Postprandial fullness. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.;Early Satiety. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.;Bloating. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.;Nausea. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.;Belching. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.