Randomised controlled trial comparing biofeedback training and specific bladder neck effective pelvic floor rehabilitation in stress urinary incontinent wome

Not Applicable

Recruiting

• Conditions: N39.3; N39.42; N81.1; Stress incontinence; Cystocele

• Registration Number: DRKS00004218
• Lead Sponsor: Charité Universitätsmedizin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-08-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 108

Inclusion Criteria

Motivation to undergo conservative treatment

Exclusion Criteria

neurological diseases, inability to understand German

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement of pelvic floor symptoms /quality of life employing validated pelvic floor questionnaire at all clinical posttherapeutic visits (after 6 weeks, after 6 months, after 1 year)

Secondary Outcome Measures

Name	Time	Method
Evaluation of pelvic floor pre-contraction, bladder neck elevation, pelvic floor muscle configuration, length of pelvic floor contraction applying perineal ultrasound at all scheduled follow up appointments (after 6 weeks, after 6 months, after 1 year)