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Intravaginal Laser Treatment of Mild and Moderate Stress Incontinence

Not Applicable
Completed
Conditions
Stress Incontinence, Female
Interventions
Device: laser therapy
Registration Number
NCT03267719
Lead Sponsor
University Hospital Tuebingen
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
30
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
laser therapylaser therapyErbium-laser therapy will be applied
Primary Outcome Measures
NameTimeMethod
Quality of life6 month

Quality of life will be access via ICIQ-SF questionaire

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department for Women's Health

🇩🇪

Tübingen, Germany

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