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PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial Neuromodulation System in Patients With OAB — RESET  

Overactive Bladder Clinical Trial

Official title:
PRospective Study to Evaluate EffectivenesS With the NURO™ PErcutaneous Tibial Neuromodulation (PTNM) System in Patients With OAB

Clinical Trial Summary

To evaluate the NURO system for the treatment of OAB in drug naïve patients.

Clinical Trial Description

The purpose of this prospective, multicenter, single arm study is to evaluate the NURO system for the treatment of OAB in drug naïve patients. The study will assess change from baseline through 12 PTNM therapy sessions in UUI (urge urinary incontinence) episodes, voiding episodes, and patient reported outcomes. The study is expected to last approximately 14 weeks per subject following the enrollment visit. Subjects will be exited from the study after the final study visit is complete. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02857816
Study type Interventional
Source MedtronicNeuro
Contact
Status Completed
Phase N/A
Start date September 2016
Completion date November 21, 2017
View Details
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