MedPath

Surgery for women with pelvic organ prolapse

Not Applicable
Conditions
Vaginal wall prolapse
Urological and Genital Diseases
Female genital prolapse
Registration Number
ISRCTN60695184
Lead Sponsor
niversity of Aberdeen (UK)
Brief Summary

2016 results in https://www.ncbi.nlm.nih.gov/pubmed/28010989

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
Female
Target Recruitment
4500
Inclusion Criteria

Women (no age limits) having primary or secondary pelvic organ prolapse surgery for anterior and/or posterior vaginal wall prolapse who are willing and eligible to be randomised

Notes:
1. Women who are unwilling or ineligible for randomisation will be eligible to be followed up using the same protocol as part of the comprehensive cohort
2. Women undergoing concurrent hysterectomy/cervical amputation, vault surgery or continence procedures are also eligible

Exclusion Criteria

1. Women undergoing prolapse surgery who are unwilling or unable to participate in the study
2. Women who are unable or unwilling to give competent informed consent, or are unable to complete study questionnaires

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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