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Neuspera Revision Registry - Follow up Revision Experience and Evaluation of Device Outcomes Metrics
Sponsor: Neuspera Medical, Inc.
Summary
Single-arm study where subjects' responses to a questionnaire for the traditional Sacral Neuromodulation (SNM) devices will be compared to the responses regarding the Neuspera SNM System.
Official title: Follow-up Revision Experience and Evaluation of Device Outcomes Metrics in Subjects Receiving Replacement of Traditional Sacral Neuromodulation (SNM) With the Neuspera SNM System
Key Details
Gender
All
Age Range
22 Years - Any
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2026-04-01
Completion Date
2027-04
Last Updated
2026-10-14
Healthy Volunteers
No
Conditions
Interventions
Neuspera Implantable Sacral Neuromodulation System
Stimulation of the Sacral Nerve
Locations (1)
Specialty Clinical Research of St. Louis
St Louis, Missouri, United States