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RecruitingNCT06497647

New Treatment for Nocturnal Enuresis in Children

Outcome of Treatment of Monosymptomatic Nocturnal Enuresis in Children Using Imipramine Alone Versus Sulbutiamine Alone Versus Imipramine Plus Sulbutiamine : Prospective Comparative Study

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
450 (estimated)
Sponsor
Sohag University · Academic / Other
Sex
All
Age
6 Years – 18 Years
Healthy volunteers
Accepted

Summary

The aim of the study is to evaluate the role of sulbutiamine in treatment of monosymptomatic nocturnal enuresis in children by using it alone or as a combination therapy with tricyclic antidepressants (imipramine+sulbutiamine).

Conditions

Interventions

TypeNameDescription
DRUGSulbutiaminesulbutiamine will be used by oral route 100 mg daily for 1 month and follow up will be done every 1 month till 3 months. it will be used alone in group B and combined with imipramine in group C
DRUGImipramineimipramine will be used by oral route 25 mg daily for 1 month and follow up will be done every 1 month till 3 months. it will be used alone in group A and combined with sulbutiamine in group C

Timeline

Start date
2024-03-01
Primary completion
2024-09-01
Completion
2024-11-01
First posted
2024-07-12
Last updated
2024-07-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06497647. Inclusion in this directory is not an endorsement.

New Treatment for Nocturnal Enuresis in Children (NCT06497647) · Clinical Trials Directory