Optimal Pulse Width Used in Transcutaneous Electrical Nerve Stimulation for Treating Nocturnal Enuresis in Children

Recruiting N/A Interventional Study
Nocturnal Enuresis Bedwetting
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
5 – 17
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
70 (estimated)
Sponsor
Albany Medical College · Other
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About This Trial
Children referred to pediatric urology clinic for primary nocturnal enuresis will be screened for enrollment. Patients who fail will next be offered therapy with a bedwetting alarm device or a TENS unit as an alternative, and those who chose TENS therapy will be included in the study.The patients will be randomized into two groups of 35 patients each.Group 1 will be the high pulse width set at 260…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Presenting with nocturnal enuresis (more than 1x a week) 2. Failed Behavioral modification treatment (limiting evening drinking, double voiding prior to bedtime, bowel habits, social anxiety factors) during the 30 day period prior to randomization 3. Ability to provide inform…
Contacts

Brenda Romeo, CCRC

518-262-3349

romeob@amc.edu

CONTACT