Clinical Trials Directory

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

TypeNameDescription
DRUGMinirinMinirin 5 to 10 mg daily for 6 months
DRUGOxybutyninOxybutynin 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.