surgery for prolapse

Not Applicable

• Conditions: Apical vaginal prolapse.; N99.3; Prolapse of vaginal vault after hysterectomy

• Registration Number: IRCT20180106038231N1
• Lead Sponsor: Kerman University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 15

Inclusion Criteria

18-75 years
Cervical prolapse
Symptomatic prolapse
no response to consevative treatment
Demand for surgical treatment for the treatment of prolapse

Exclusion Criteria

contraindication for surgery
malignancy
Active genitourinary tract infection
pregnancy and breastfeeding
hypersensitivity to mesh

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of life. Timepoint: Follow up 12 months after surgery. Method of measurement: Using a questionnaire and examination.;Sexual function. Timepoint: Follow up 12 months after surgery. Method of measurement: Using a questionnaire and examination.;Complication. Timepoint: Follow up 12 months after surgery. Method of measurement: Using a questionnaire and examination.;Sign and symptom. Timepoint: Follow up 12 months after surgery. Method of measurement: Using a questionnaire and examination.