Assesment the effect of Domperidone in the treatment of Functional Abdominal Pain in childre
Phase 3
Recruiting
- Conditions
- Functional Abdominal Pain.K59.9Functional intestinal disorder, unspecified
- Registration Number
- IRCT20160308026973N2
- Lead Sponsor
- Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
5-14 years old children referred to Amirkola Children's Hospital with diagnosis of functional abdominal pain (FAP)
Exclusion Criteria
Existence of chronic disease
Taking other medications such as antibiotice and probiotic during the month before the start of the project
The presence of Abdominal pain's red flags
Constipation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change at least 50% of the frequency of pain. Timepoint: At the beginning of the study and after two months of medication (end of the study). Method of measurement: Based on the questionnaire of reducing the frequency of pain, pain intensity and duration of pain (assessment of pain intensity based on face scale questionnaires).
- Secondary Outcome Measures
Name Time Method Abdominal pain intensity based on Wong-Baker FACES Pain Rating Scale questionnaire. Timepoint: At the beginning of the study (before the intervention) and after two months of medication (end of the study). Method of measurement: Wong-Baker FACES Pain Rating Scale questionnaire.;Duration of pain. Timepoint: At the beginning of the study (before the intervention) and after two months of medication (end of the study). Method of measurement: Attached questionnaire at the end of the proposal (based on patient statements).;Pain frequency (number of pain days per month). Timepoint: At the beginning of the study (before the intervention) and after two months of medication (end of the study). Method of measurement: Attached questionnaire at the end of the proposal (based on patient statements).