Clin2
NCT07383688Possibly a fitNot yet recruiting

FREEDOM Registry: Tracking outcomes of Neuspera SNM system

Urinary Urge Incontinence

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This study is for people who have or had a traditional device for overactive bladder (called sacral neuromodulation) and are considering switching to a newer, smaller Neuspera system. It will track how well the new device works and how patients do over time.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
22 years and older
Study type
Observational

Who can take part

  • You currently have a traditional sacral neuromodulation (SNM) device and want to switch to the Neuspera system, OR you had your traditional SNM device completely removed within the last year.
  • You are 22 years old or older.
  • You had at least 50% fewer urgency incontinence (sudden leaks) episodes during a stimulation trial or with your traditional system, shown on a bladder diary.
  • You are a good candidate for surgery and can receive the Neuspera system per its instructions.
  • You can attend all study tests and follow-up visits.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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