Effect of Poly ethylene glycol and Lactoluse on abdominal pain in childre
Phase 3
- Conditions
- abdominal pain in pediatrics.Unspecified abdominal pain
- Registration Number
- IRCT20181214041966N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 52
Inclusion Criteria
patients at the age of 4 to 18 years
patients with abdominal pain more than 14 days
patients with abdominal pain lacking ROME III criteria for constipation
patients with fecal impaction in abdominal X ray
Exclusion Criteria
Abdominal surgery
Hematochezia
Antibiotic consumption in the last 2 weeks
Laxative consumption in the last 2 weeks
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 56% of patients suffered from moderate abdominal pain. Timepoint: before intervention and 2, 3, 4, 5, 6, 8, 12 weeks after intervention. Method of measurement: pain score scale.
- Secondary Outcome Measures
Name Time Method