Clin2
NCT05200923Possibly a fitRecruiting

Testing a pelvic nerve device study for bladder and bowel leaks

Overactive BladderFecal IncontinenceUrinary Retention

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

This study checks how well an implanted pelvic nerve system works for people with bladder overactivity, non-obstructive urinary retention, or fecal incontinence. You may need to keep your current medications steady and track symptoms closely with diaries before and during evaluation.

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

Phase
N/A
Enrollment
300 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be 18 years or older
  • Your doctor has already decided you will get a Medtronic InterStim lead implant for the study-allowed reason, or you are already getting it
  • You must be able to sign consent and follow all study visits and instructions
  • You must be able to accurately fill out symptom diaries and questionnaires
  • For this trial, you generally must keep your current bladder/bowel medicine dose and schedule the same during the study evaluation period
  • Your symptom pattern must match one of the study groups based on your 3-day or first-72-hour diaries

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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