Comparison of two treatment method in children with primary nocturnal enuresis
Phase 3
- Conditions
- nocturnal enuresis.Nonorganic enuresis
- Registration Number
- IRCT20170509033894N3
- Lead Sponsor
- Vice Chancellor for Research and Technology of Ahvaz Jundishapur University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
children with primary nucturnal enurises
Exclusion Criteria
patients with neurogenic bladder
CNS disorders
urine-concentrating defects
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Response to treatment. Timepoint: Monthly regarding during 6 months. Method of measurement: According things that their parents and children say, patients will be classified to full response (complete dry), good response (90 to 99% reduction in wet nights), and partial response (50 to 90% reduction).
- Secondary Outcome Measures
Name Time Method Abdominal pain. Timepoint: Monthly during 6 months. Method of measurement: Clinical symptoms.;Vomiting. Timepoint: Monthly during 6 months. Method of measurement: Clinical symptoms.