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Clinical Trials/NCT03693690
NCT03693690
Recruiting
Not Applicable

Far Eastern Memorial Hospital

Far Eastern Memorial Hospital1 site in 1 country200 target enrollmentOctober 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laser Thermotherapy, Stress Urinary Incontinence
Sponsor
Far Eastern Memorial Hospital
Enrollment
200
Locations
1
Primary Endpoint
Global response assessment
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The main aim of this study is to elucidate factors affecting treatment efficacy of vaginal laser therapy.

Detailed Description

Laser thermotherapy can increase the stiffness of vaginal wall. It has been reported that vaginal laser therapy can be used to treat stress urinary incontinence. However, factor affecting treatment efficacy of vaginal laser therapy remains unknown. Thus the main aim of this study is to elucidate factors affecting treatment efficacy of vaginal laser therapy. Besides, the durability of vaginal laser therapy will be assessed. The above knowledge should be helpful for clinical decision making.

Registry
clinicaltrials.gov
Start Date
October 1, 2018
End Date
December 31, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sheng-Mou Hsiao

Chief, Department of Obstetrics & Gynecology

Far Eastern Memorial Hospital

Eligibility Criteria

Inclusion Criteria

  • \>20 years old female
  • had stress urinary incontinence symptoms
  • Sexual behavior
  • No urinary tract infection
  • At their own expense for vaginal laser therapy

Exclusion Criteria

  • Abnormal vaginal bleeding
  • Vaginal fistula

Outcomes

Primary Outcomes

Global response assessment

Time Frame: 2 years

Secondary Outcomes

  • Duration of sustained efficacy(2 years)

Study Sites (1)

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