MedPath

Fractional CO2 laser treatment for women with stress urinary incontinence: A randomized controlled trial

Not Applicable
Conditions
female stress urinary incontinence
CO2 laser&#44
To evaluate the efficacy of CO2 laser for treating SUI patients
Registration Number
TCTR20190131004
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
Female
Target Recruitment
54
Inclusion Criteria

Patients with SUI

Exclusion Criteria

1.patients with pelvic organ prolapse more than stage I. That is the maximum prolapse is at 1 cm above hymen or below this point
2.patients who have recurrent cystitis
3.patients who have undergone anti-incontinence surgery before
4.patients whose BMI>30 kg/m2
5. pregnancy
6.patients who have vaginal pathology or current infection
7.patients who have abnormal uterine bleeding with unknown cause
8.laser allergy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptoms improvement of stress urinary incontinence before intervention, finish intervention and 3 month later Using Questionnaire
Secondary Outcome Measures
NameTimeMethod
Pelvic organ prolapse quantification and organ descent from translabial ultrasound before intervention, finish intervention and 3 month later Physical examination and transperineal ultrasound measurement
© Copyright 2025. All Rights Reserved by MedPath