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Study of 30-Minute Stimulation With the Neuspera Sacral Neuromodulation (SNM) System

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Enrollment target: 20 to 30
    • Study description revised
    v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Primary endpoints revised (2)
    • Study sites: 0 to 1
    • Start date changed from estimate of Nov 2025 to Nov 19, 2025
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Single-arm study conducted in participants for the treatment of urinary urge incontinence in patients who have failed, could not tolerate, or were not a candidate for more conservative treatments. The objective of the study is to assess the effectiveness of 30-minutes daily therapeutic stimulation with the Neuspera System.
Trial Details
NCT Number NCT07247136
Lead Sponsor Neuspera Medical, Inc.
Conditions
(from sponsor)		 Urinary Urge Incontinence
Related terms Urinary Incontinence, Urge
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov