Functional dyspepsia. Indigestion
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity Assessment of Dyspepsia. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahed University of Medical Sciences