Fractional CO2 laser treatment for women with stress urinary incontinence: A randomized controlled trial
Not Applicable
- Conditions
- female stress urinary incontinenceCO2 laser,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
Name Time Method Symptoms improvement of stress urinary incontinence before intervention, finish intervention and 3 month later Using Questionnaire
- Secondary Outcome Measures
Name Time Method Pelvic organ prolapse quantification and organ descent from translabial ultrasound before intervention, finish intervention and 3 month later Physical examination and transperineal ultrasound measurement