← Eichor
Study identifier: NCT07144813 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-Approval Study of the Neuspera Sacral Neuromodulation System

Condition: Urinary Urgency Incontinence  ·  Sponsor: Neuspera Medical, Inc.

PhaseNA
Planned participants116
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Mark Vollmer  ·  408-433-3839  ·  mark.vollmer@neuspera.com

Shital Patel  ·  323-528-1320  ·  shital.patel@neuspera.com

Always discuss trial participation with your own doctor first.

Locations (20)

Kaiser Permanente Point Loma MOBSan Diego, California, United StatesActive Not Recruiting
Genesis Healthcare PartnersSan Diego, California, United StatesActive Not Recruiting
Florida Urology PartnersTampa, Florida, United StatesActive Not Recruiting
Women's Health Advantage,Fort Wayne, Indiana, United StatesActive Not Recruiting
Indiana University, School of MedicineIndianapolis, Indiana, United StatesActive Not Recruiting
University of Kansas Medical Center,Kansas City, Kansas, United StatesActive Not Recruiting
University of Louisville Health System,Louisville, Kentucky, United StatesActive Not Recruiting
Ochsner MedicalNew Orleans, Louisiana, United StatesActive Not Recruiting
University of Michigan HealthWyoming, Michigan, United StatesActive Not Recruiting
Minnesota UrologyWoodbury, Minnesota, United StatesActive Not Recruiting
Specialty Research of St. LouisSt Louis, Missouri, United StatesActive Not Recruiting
Adult & Pediatric Urology P.COmaha, Nebraska, United StatesActive Not Recruiting

+ 8 more locations — full list on the registry record.

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07144813