Comparison of the efficacy of two therapeutic regimens for primary nocturnal enuresis; oxybutnin plus desmopressin versus desmopressin in pediatric patients
Not Applicable
- Conditions
- Primary nocturnal enuresis.Nonorganic enuresis
- Registration Number
- IRCT201301117892N4
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
(5 to 18 year-old patients with primary nocturnal enuresis)
Exclusion criteria: (to have neurogenic bladder; CNS disorders; secondary nocturnal enuresis; occurrence of drug side effects)
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 12 weeks. Method of measurement: Using a questionnaire.
- Secondary Outcome Measures
Name Time Method