Neurogenic Bladder Clinical Trials

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A Randomized Control Trial of Transcutaneous Tibial Nerve Stimulation for Neurogenic Bladder in the Pediatric Population

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to determine the safety, feasibility, and compliance of a daily home transcutaneous tibial nerve stimulation (tTNS) protocol in children with chronic neurogenic bladder (NB) provided by self or caregiver for 4 weeks and to estimate the efficacy of tTNS

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Maximum Age: 17
Healthy Volunteers: f
View:

• chronic neurogenic bladder

• Spina Bifida diagnosis

• Use of overactive bladder medication(s)

• Stable bladder medications for ≥ 3 months

Locations
United States
Texas
The University of Texas Health Science Center and Houston
RECRUITING
Houston
Contact Information
Primary
Argyrios Stampas, MD, MS
Argyrios.Stampas@uth.tmc.edu
(713) 797-5007
Backup
Jaqueline Martinez
Jacqueline.B.Martinez@uth.tmc.edu
713-797-5765
Time Frame
Start Date: 2026-03-27
Estimated Completion Date: 2027-08-11
Participants
Target number of participants: 20
Treatments
Experimental: Stamobil electric stimulator
Sham_comparator: sham tTNS device
Related Therapeutic Areas
Sponsors
Leads: The University of Texas Health Science Center, Houston

This content was sourced from clinicaltrials.gov