Evaluation of Non-Wheat gluten Diet in Chidren and Adolescents With Functional Abdominal Pai

Phase 2

Recruiting

• Conditions: Functional abdominal pain.

• Registration Number: IRCT20190410043224N2
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Children with functional abdominal pain according to the criteria of Rome 4 in the ages of 12 to 18 years, referred to the subspecialty gastroenterology clinics of Isfahan University of Medical Sciences with the conditions.. ......
Do not take steroids or nonsteroidal anti-inflammatory drugs or any other medication for 2 weeks before endoscopic examination
Patients who are not on medication(Do not take steroids / antacids / proton pump inhibitors / probiotics / nonsteroidal anti-inflammatory drugs / antidepressants and antipsychotics)
Patients who have not been on a gluten-free / gluten-free diet for the past 6 months
Lack of sensitivity to wheat
Absence of other organic diseases of the gastrointestinal tract (celiac disease, inflammatory bowel disease .......)
Absence of abdominal surgery (intestinal resection)
Absence of diseases, infectious / diabetes mellitus / systemic autoimmune / immunodeficiency / psychological disorders
No previous anaphylactic reaction attacks
Negative Anti endomysial Ab test

Exclusion Criteria

Children with abdominal pain with organic causes.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Functional abdominal pain. Timepoint: In both groups before the intervention and three weeks after the intervention and three weeks after the Wash out. Method of measurement: Check list and questionaire.

Secondary Outcome Measures

Name	Time	Method
In each stage of filling out the checklist, In addition to abdominal pain, variables of diarrhea, bloating, body pain, limb pain, anxiety, headache, and feeling unwell are also evaluated.. Timepoint: In both groups before the intervention and three weeks after the intervention and three weeks after Wash out. Method of measurement: Checklist and questionnaire.