The effect of pessary on the clinical care of women with prolapse
Not Applicable
Recruiting
- Conditions
- terine prolapse.
- Registration Number
- IRCT20110425006284N17
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 72
Inclusion Criteria
Women aged 45-60 years
Married women and women living together with their husbands
Literacy
Willingness and interest in participating in the study
Minimal first-degree prolapse
Tendency to use pessary instead of surgery
Lack of vaginitis
Exclusion Criteria
Having vaginal discharge and infection and the patient's unwillingness For pessary placement..
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Correction of uterine prolapse. Timepoint: At the beginning of the study (before the intervention) and once 8 weeks after the intervention. Method of measurement: Pelvic Organ Prolapse Quantification (POP-Q) System.
- Secondary Outcome Measures
Name Time Method Quality of life and sexual self-efficacy and management of patient clinical care. Timepoint: Once at the beginning of the study (before the intervention) and once 8 weeks after the intervention. Method of measurement: Quality of Life Questionnaire in Women with Prolapse (P-QOL), Vaziri and Lotfi Self-Efficacy Questionnaire, PGI Three-Question Scale Questionnaire, Researcher-Managed Clinical Care Questionnaire.