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Completed Not applicable Interventional Results available

BlueWind RENOVA iStim™ System for the Treatment of OAB

ClinicalTrials.gov ID: NCT03596671

Public ClinicalTrials.gov record NCT03596671. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 9:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective Study to Assess the Efficacy and Safety of the BlueWind RENOVA iStim™ System in the Treatment of Patients Diagnosed With Overactive Bladder (OASIS - OverActive Bladder StImulation System Study)

Study identification

NCT ID
NCT03596671
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
BlueWind Medical
Industry
Enrollment
282 participants

Conditions and interventions

Interventions

  • RENOVA iStim™ System Device

Device

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 11, 2019
Primary completion
Oct 27, 2022
Completion
Jan 23, 2025
Last update posted
Sep 15, 2025

2019 – 2025

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
University of California Irvine Orange California 92868
Kaiser Permanente San Diego California 92110
Norwalk Urology Norwalk Connecticut 06850
Florida Urology Partners Tampa Florida 33615
Comprehensive Urologic Care Lake Barrington Illinois 60010
Regional Urology, LLC Shreveport Louisiana 71106
Chesapeake Urology - Hanover Hanover Maryland 21076
Chesapeake Urology - Owing Mills Owings Mills Maryland 21117
Minnesota Urology Woodbury Minnesota 55125
Adult Pediatric Urology & Urogynecology Omaha Nebraska 68114
Duke Urogynecology Durham North Carolina 27707
Southern Urogynocology West Columbia South Carolina 29169
Sanford Health Sioux Falls South Dakota 57105
University of Washington Seattle Washington 98195

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03596671, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 15, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03596671 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →