Comparison of the effectiveness of medicinal and non-medicinal therapy on the control of nocturnal enuresis of childre

Phase 2

Recruiting

• Conditions: urinary incontinence.; Functional urinary incontinence; R39.81

• Registration Number: IRCT20180428039453N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 September 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

children with primary enuresis with 6 to 18 years old
completion of informed consent form no existence of urological diseases

Exclusion Criteria

patients with neurogenic bladder congenital disorders of urinary system urinary tract obstruction neurological disorders such as myelomenoncule unwillingness to participate in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of control and improvement of incontinence after use of enuresis alarm vs desmopressin. Timepoint: A month after use of enuresis alarm. Method of measurement: The therapeutic response will be divided into three levels more effectively and without any difference and less effect.