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NCT07144813 · ClinicalTrials.gov registry record · NA
Post-Approval Study of the Neuspera Sacral Neuromodulation System
A NA study of Urinary Urgency Incontinence, sponsored by Neuspera Medical.
- Recruiting
- Registry status
- NA
- Development phase
- 116
- Enrollment target
- 20
- Study locations
NCT07144813 is a NA study of Urinary Urgency Incontinence that is actively recruiting participants, run by Neuspera Medical. The registered enrollment target is 116 participants. The trial reports 20 study locations across 17 states.
The verdict
NCT07144813, a NA study of Urinary Urgency Incontinence, is actively recruiting participants, sponsored by Neuspera Medical.
- RECRUITING
- Registry status
- NA
- Development phase
- 116 participants
- Enrollment target
- 20
- Study locations
Study Summary
Prospective, multi-center, single-arm, post-approval study is designed to assess the long-term safety and efficacy data of the Neuspera Sacral Neuromodulation (SNM) System following commercial approval of the Neuspera SNM System. Participants in this study received intervention/implanted in Phase I or Phase II of the Neuspera SANS\_UUI (NSM-004) Study.
Conditions Studied
Interventions
- DEVICE Neuspera Implantable Sacral Neuromodulation System
Study Locations (20)
California
- Kaiser Permanente Point Loma MOB - San Diego
- Genesis Healthcare Partners - San Diego
Indiana
- Women's Health Advantage, - Fort Wayne
- Indiana University, School of Medicine - Indianapolis
Texas
- Urology Austin, - Austin
- UCNT Dallas, - Dallas
Florida
- Florida Urology Partners - Tampa
Kansas
- University of Kansas Medical Center, - Kansas City
Kentucky
- University of Louisville Health System, - Louisville
Louisiana
- Ochsner Medical - New Orleans
Michigan
- University of Michigan Health - Wyoming
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 116 participants |
| Start Date | 2025-09-03 |
| Est. Completion | 2029-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07144813
The ClinicalTrials.gov registry entry for NCT07144813 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 116 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neuspera Medical, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urinary Urgency Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Neuspera Implantable Sacral Neuromodulation System is the first listed.
NCT07144813 reports 20 study locations spanning 17 distinct geographic areas - top geographies include California, Indiana, Texas.
Frequently Asked Questions
What is clinical trial NCT07144813 about?
NCT07144813 is a clinical study titled "Post-Approval Study of the Neuspera Sacral Neuromodulation System". Prospective, multi-center, single-arm, post-approval study is designed to assess the long-term safety and efficacy data of the Neuspera Sacral Neuromodulation (SNM) System following commercial approval of the Neuspera SNM System. Participants in this study received intervention/implanted in Phase I...
What is the current status of trial NCT07144813?
This trial is currently recruiting. It is a NA study. The enrollment target is 116 participants. The study started on 2025-09-03. Estimated completion is 2029-12.
What conditions does trial NCT07144813 study?
This clinical trial studies the following conditions: Urinary Urgency Incontinence.
What interventions are being tested in trial NCT07144813?
The interventions under investigation include: Neuspera Implantable Sacral Neuromodulation System (DEVICE).
Who is sponsoring clinical trial NCT07144813?
This trial is sponsored by Neuspera Medical, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07144813 being conducted?
This trial has 20 study locations across California, Florida, Indiana, Kansas, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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