A scale used for assesement of amount of female genital prolapse who are planned for removal of uterus vaginally before and after the surgical repair

Not Applicable

• Conditions: Health Condition 1: N813- Complete uterovaginal prolapse

• Registration Number: CTRI/2020/12/029560
• Lead Sponsor: nil

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

all patient admitted for pelvic floor repair surgery in kasturba hospital manipal

Exclusion Criteria

Patients unfit for surgery due to medical and other co moralities. Patients with ring pessary in situ

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To measure the extent of anatomical correction achieved by pelvic reconstruction surgeryTimepoint: 2 years

Secondary Outcome Measures

Name	Time	Method
Quality of Life post pelvic floor repairTimepoint: 2 years