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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Study of Urgent PC Versus Sham Effectiveness in Treatment of Overactive Bladder Symptoms

ClinicalTrials.gov ID: NCT00771264

Public ClinicalTrials.gov record NCT00771264. 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 Oct 25, 2026, 3:05 PM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to demonstrate superiority of percutaneous posterior tibial nerve stimulation (PTNS) therapy compared to sham therapy for the treatment of patients with overall bladder (OAB) symptoms.

Study identification

NCT ID
NCT00771264
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Uroplasty, Inc
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Sep 2008 (Type not available)
Primary completion
Jun 2009 (Actual)
Completion
Jun 2009 (Actual)
Last update posted
Apr 18, 2012

2008 – 2009

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Gregory L. Davis, M.D., FACOG, Inc. Chico California 95928 —
Greenwich Urological Associates, P.C. Greenwich Connecticut 06830 —
Specialists in Urology Naples Florida 34102 —
Mercy Health Partners at the Lakes Muskegon Michigan 49444 —
Beaumont Hospital Royal Oak Michigan 48703 —
Grand Rapids Women's Health DBA Female Pelvic Medicine & Urogynecology Institue of Michigan Grand Rapids Minnesota 49503 —
Uroplasty, Inc Minnetonka Minnesota 55343 —
Beaumont Hospital Royal Oak Minnesota 48073 —
Urology Health Center, PC Fremont Nebraska 68025 —
Capital Region Urological Surgeons, PLLC Albany New York 12208 —
Central Missouri Women's Healthcare, LLC White Plains New York 10604 —
Alliance Urology Specialists Greensboro North Carolina 27403 —
University of Oklahoma Oklahoma City Oklahoma 73104 —
Virginia Urology Richmond Virginia 23235 —
Athena Urology Issaquah Washington 98027 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00771264, 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 Apr 18, 2012 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00771264 live on ClinicalTrials.gov.

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