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Post-Approval Study of the Neuspera Sacral Neuromodulation System

RecruitingNAAges 22 Years - anyAllNeuspera Medical, Inc.
NCT07144813 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Subjects in the SANS-UUI Phase I or Phase II study Exclusion Criteria: * None
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What it tests

  • Neuspera Implantable Sacral Neuromodulation System
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Where

20 sites
Kaiser Permanente Point Loma MOB
San Diego, United States
Genesis Healthcare Partners
San Diego, United States
Florida Urology Partners
Tampa, United States
Women's Health Advantage,
Fort Wayne, United States
Indiana University, School of Medicine
Indianapolis, United States
University of Kansas Medical Center,
Kansas City, United States
University of Louisville Health System,
Louisville, United States
Ochsner Medical
New Orleans, United States

…and 12 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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