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Prospective Evaluation of Keat Electrostimulator in the Auto-reeducation of Female Urinary Incontinence

NCT01276340 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 450

Last updated 2012-05-17

No results posted yet for this study

Summary

The investigators performed a prospective analysis of 450 women with stress, urge and mixed incontinence in order to assess the health-related quality of life (Contilife® questionnaire) and the objective cure rate after two months of electrical stimulation (Keat® stimulator). Management of urinary incontinence with the Keat® stimulator could given an improvement in the quality of life and a good rate of satisfaction without side effect.

Objective cure is as good as subjective improvement especially in urinary stress incontinence. Keat® stimulator is a non-invasive and simple new technique that could be the bew first-line non surgical treatment for female urinary incontinence.

Conditions

Interventions

DEVICE

KEAT stimulator

electrical stimulation with KEAT stimulator : 4 times per week during 2 months

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Saint Etienne

    lead OTHER

Principal Investigators

  • Gautier CHENE, MD · CHU de Saint-Etienne

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2011-12-31
Completion
2012-02-29

Countries

  • France

Study Locations

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Entities

Diseases

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 NCT01276340 on ClinicalTrials.gov