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NCT07792031Possibly a fitNot yet recruiting

Pelvic floor device comparison for women with urinary incontinence

Urinary IncontinenceMixed Urinary IncontinenceUrinary Incontinence (UI)Stress Urinary Incontinence (SUI)Stress Urinary Incontinence in Women

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

This trial compares two types of pelvic floor muscle stimulation devices to see which one works better in reducing urine leakage in women with mixed urinary incontinence (a combination of stress and urge incontinence). Participating might help you find an effective, non-drug treatment option.

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

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

Who can take part

  • You are a woman aged 18 or older.
  • You have mixed urinary incontinence (leakage with both cough/sneeze and sudden urge) for at least 3 months.
  • You experience at least 2 and up to 5 leaks in a 3-day diary at the start of the study.
  • You have not taken medications for overactive bladder or incontinence in the last 8 weeks, and have not had pelvic floor training, electrical stimulation, or similar treatments (preferably never).
  • You are able to attend all 12 treatment sessions and fill out bladder diaries and questionnaires.
  • You do not have an active urinary tract infection, visible blood in urine, severe pelvic organ prolapse (stage III-IV), are not pregnant or less than 2 months postpartum, and do not have a major neurological disease affecting bladder function.

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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