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Clinical Trials/NCT02178735
NCT02178735
Completed
Phase 4

Clinical Outcomes and Urodynamic Effects After Vaginal Tailored Mesh Surgery for Pelvic Organ Prolapse

National Taiwan University Hospital1 site in 1 country104 target enrollmentMay 2014

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Pelvic Organ Prolapse
Sponsor
National Taiwan University Hospital
Enrollment
104
Locations
1
Primary Endpoint
Recurrence of pelvic organ prolapse
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

To evaluate the clinical outcome and urodynamic effect of two novel vaginal tailored mesh surgeries.

Detailed Description

We will review the medical records (including medical data, urodynamic data, pad weight data, etc) of women who underwent either anterior or posterior novel vaginal tailored mesh surgeries at National Taiwan University Hospital between November 2011 and November 2013.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All women with pelvic organ prolapse who underwent either anterior or/and posterior vaginal tailored mesh surgeries in National Taiwan University Hospital between November 2011 and November 2013

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Recurrence of pelvic organ prolapse

Time Frame: 1 year

Recurrence rate of cystocele, rectocele, uterine prolapse, or vaginal vault prolapse within 1 year after surgery

Secondary Outcomes

  • Vaginal mesh erosion(1 year)
  • The change of pad weight(3 months)
  • The change of maximum urethral closure pressure(3 months)

Study Sites (1)

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