Evaluation of probiotics effect on non-organic chronic Abdominal pain in childre

Not Applicable

• Conditions: on-organic chronic abdominal pain in children.

• Registration Number: IRCT201205219825N1
• Lead Sponsor: Mashhad university of medical sciencese

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 52

Inclusion Criteria

All children from 4 to 18 years with gastrointestinal functional disorder consistent with ROME III criteria are entered the test. Children under the age of 4 or over 18, whom are received the drug for the treatment of chronic pain (such as drug treatment, such as herbal medicines or probiotics), or receiving drugs that are known as cause abdominal pain, are excluded from the study.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Abdominal pain improvement. Timepoint: Every week to 4 weeks. Method of measurement: By patients and parents - Questionnare forms.

Secondary Outcome Measures

Name	Time	Method
Daily activity improvement. Timepoint: Every week to 4 weeks. Method of measurement: By patients and parents - Questionnare forms.;Change of defication. Timepoint: Every week to 4 weeks. Method of measurement: By patients and parents - Questionnare forms.;Change in appetite. Timepoint: Every week to 4 weeks. Method of measurement: By patients and parents - Questionnare forms.