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Efficacy and Safety of Extracorporeal Biofeedback

NCT00910338 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2019-12-02

No results posted yet for this study

Summary

Stress urinary incontinence is the most common type of female incontinence. The efficacy of pelvic floor muscle training with biofeedback has been already proved in many studies. But intravaginal probe is one of the limitation. So, the purpose of this study is to assess the efficacy and safety of extracorporeal biofeedback device with pelvic floor muscle training.

Conditions

  • Female Stress Urinary Incontinence

Interventions

DEVICE

PFMT with Extracorporeal Biofeedback

Pelvic Floor Muscle Training with Extracorporeal Biofeedback Device for 12 weeks * Twice a week for the first 4 weeks * Once a week for the next 8 weeks

Sponsors & Collaborators

  • Furun Medical

    collaborator INDUSTRY

  • KYU-SUNG LEE

    lead OTHER

Principal Investigators

  • Kyu-Sung Lee, Ph.D · Samsung Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2009-03-31
Completion
2009-12-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00910338 on ClinicalTrials.gov