The effectiveness of vaginal radiofrequency in preventing the prolapse of pelvic organs after surgery
Phase 2
Recruiting
- Conditions
- Pelvic organ prolapse.Female genital prolapse
- Registration Number
- IRCT20220906055897N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Patients with pelvic organ prolapse
Exclusion Criteria
Patients with active or recurrent genital infection (genital herpes, candidiasis)
Recurrent urinary tract infection
History of pelvic radiotherapy or vaginal brachytherapy
History of reconstructive pelvic surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The degree of pelvic organ prolapse. Timepoint: Before, 6, 10, 14 and 18 weeks after surgery. Method of measurement: The pelvic organ prolapse quantifications system (POP-Q).;Quality of life. Timepoint: Before, 6, 10, 14 and 18 weeks after surgery. Method of measurement: Pelvic floor distress inventory (PFDI-20).
- Secondary Outcome Measures
Name Time Method Sexual satisfaction. Timepoint: Before, 6, 10, 14 and 18 weeks after surgery. Method of measurement: The female sexual function index (FSFI).