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Recruiting Not applicable Interventional

Post-Approval Study of the Neuspera Sacral Neuromodulation System

ClinicalTrials.gov ID: NCT07144813

Public ClinicalTrials.gov record NCT07144813. 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, 3:41 AM EDT

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

Official title

Clinical Post- Approval Study of the Neuspera Sacral Neuromodulation (SNM) System in Patients With Symptoms of Urinary Urgency Incontinence (UUI)

Study identification

NCT ID
NCT07144813
Recruitment status
Recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Neuspera Medical, Inc.
Industry
Enrollment
116 participants

Conditions and interventions

Interventions

  • Neuspera Implantable Sacral Neuromodulation System Device

Device

Eligibility (public fields only)

Age range
22 Years and older
Sex
All
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
Sep 2, 2025
Primary completion
Nov 30, 2029
Completion
Nov 30, 2029
Last update posted
Feb 3, 2026

2025 – 2029

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Kaiser Permanente Point Loma MOB San Diego California 92110 Active, not recruiting
Genesis Healthcare Partners San Diego California 92123 Active, not recruiting
Florida Urology Partners Tampa Florida 33615 Active, not recruiting
Women's Health Advantage, Fort Wayne Indiana 46825 Active, not recruiting
Indiana University, School of Medicine Indianapolis Indiana 46202 Active, not recruiting
University of Kansas Medical Center, Kansas City Kansas 66160 Active, not recruiting
University of Louisville Health System, Louisville Kentucky 40202 Active, not recruiting
Ochsner Medical New Orleans Louisiana 70121 Active, not recruiting
University of Michigan Health Wyoming Michigan 49519 Active, not recruiting
Minnesota Urology Woodbury Minnesota 55125 Active, not recruiting
Specialty Research of St. Louis St Louis Missouri 63141 Active, not recruiting
Adult & Pediatric Urology P.C Omaha Nebraska 68114 Active, not recruiting
Premier Medical Group, Poughkeepsie New York 12603 Active, not recruiting
MetroHealth System, Cleveland Ohio 44109 Active, not recruiting
Women's Healthcare Associates, Portland Oregon 97225 Active, not recruiting
The Institute for Female Pelvic Medicine and Reconstructive Surgery, North Wales Pennsylvania 19454 Active, not recruiting
Southern Urogynecology, West Columbia South Carolina 29169 Active, not recruiting
Urology Austin, Austin Texas 78759 Recruiting
UCNT Dallas, Dallas Texas 75231 Active, not recruiting
Virginia Mason Medical Center, Seattle Washington 98101 Active, not recruiting

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 NCT07144813, 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 Feb 3, 2026 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07144813 live on ClinicalTrials.gov.

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