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The effect of Specific Dietary Interventions in Postprandial Distress Syndrom

Assessment of effect of Specific Dietary Interventions on severity of Dyspepsia in patients with Postprandial Distress Syndrom

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050322049N1
Enrollment
60
Registered
2015-08-06
Start date
2015-06-22
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functional dyspepsia. Indigestion

Interventions

Intervention 1: Intervention group: special diet based on the recommendations of the Traditional Iranian Medicine for Two weeks. In this diet, based on

Sponsors

Shahed University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

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

MeasureTime frame
Severity Assessment of Dyspepsia. Timepoint: At baseline, 2 and 8 weeks after starting the intervention. Method of measurement: The Gastrointestinal Symptom Scale.

Secondary

MeasureTime 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

Public ContactFereshteh Nouri

Shahed University of Medical Sciences

fdr.nouri@gmail.com+98 21 2288 2521

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026