Comparison of two regimens in the treatment of nocturnal enuresis
Not Applicable
- Conditions
- Primary nocturnal enuresis.Nonorganic enuresis
- Registration Number
- IRCT2012090610758N1
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
(having primary nocturnal enuresis; not having secondary nocturnal risk factors such as urinary tract infection, constipation, Diabetes Mellitus, Diabetes Insipidus, obstruction of the urinary tract, neurogenic bladder and positive history of seizure; to be between 5 to 16 years old)
Exclusion criteria: (having abnormal sonographic or urine analysis results; occurrence of side effects or missing the intake of more than two doses of the prescribed drugs)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of nocturnal urination in a week. Timepoint: weekly for four weeks. Method of measurement: Using a questionnaire.
- Secondary Outcome Measures
Name Time Method Occurrence of side effects. Timepoint: Weekly for four weeks. Method of measurement: Physical examination by a specialist.