Trials / Completed
CompletedNCT02538302
Minirin Versus Oxybutynin for Nocturnal Enuresis in Children
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 66 (actual)
- Sponsor
- Hormozgan University of Medical Sciences · Academic / Other
- Sex
- All
- Age
- 5 Years – 14 Years
- Healthy volunteers
- Not accepted
Summary
Nocturnal enuresis is among the most common disorders in children. The aim of current study was to compare the efficacy and safety of Minirin and oxybutynin for treatment of nocturnal enuresis in children in Bandar Abbas in 2014.
Detailed description
Nocturnal enuresis is among the most common disorders in children. Several pharmacological and non-pharmacological treatments are available for nocturnal enuresis. Studies for reaching the best pharmacological treatment for this disorder are continuing. The aim of current study was to compare the efficacy and safety of Minirin and oxybutynin for treatment of nocturnal enuresis in children in Bandar Abbas in 2014.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Minirin | Minirin 5 to 10 mg daily for 6 months |
| DRUG | Oxybutynin | Oxybutynin 5 to 10 mg daily for 6 months |
Timeline
- Start date
- 2013-07-01
- Primary completion
- 2015-07-01
- Completion
- 2015-08-01
- First posted
- 2015-09-02
- Last updated
- 2015-09-02
Locations
1 site across 1 country: Iran
Source: ClinicalTrials.gov record NCT02538302. Inclusion in this directory is not an endorsement.