Skip to main content
Clinical Trials/NCT03267719
NCT03267719
Completed
Not Applicable

Intravaginal Laser Treatment of Mild and Moderate Stress Incontinence

University Hospital Tuebingen1 site in 1 country30 target enrollmentAugust 31, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress Incontinence, Female
Sponsor
University Hospital Tuebingen
Enrollment
30
Locations
1
Primary Endpoint
Quality of life
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of the study is to evaluate the effectiveness of laser therapy as a non-surgical treatment option in patients with mild and moderate stress incontinence.

Detailed Description

The aim of the study is to evaluate the effectiveness of laser therapy as a non-surgical treatment option in patients with mild and moderate stress incontinence.

Registry
clinicaltrials.gov
Start Date
August 31, 2017
End Date
September 1, 2018
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Light or moderate stress incontinence
  • mixed urine incontinence with predominance of the stress component
  • written informed consent

Exclusion Criteria

  • Pregnancy
  • patients treated radiotherapy in the small basin
  • connective tissue disorders (e.g., Ehlers-Danlos syndrome, Marfan syndrome)
  • patient with or after malignant disease of the uterus, ovaries, vagina and vulva
  • former surgery due to stress incontinence (except for the patients who had a TVT insert with removal of the TVT)
  • Descensus genitalis\> POPQ Stage 1
  • former surgery due to a genital lowering with vaginal netting

Outcomes

Primary Outcomes

Quality of life

Time Frame: 6 month

Quality of life will be access via ICIQ-SF questionaire

Study Sites (1)

Loading locations...

Similar Trials