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Clinical Trials/NCT01392417
NCT01392417
Completed
Not Applicable

Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

Western Galilee Hospital-Nahariya2 sites in 1 country140 target enrollmentFebruary 2009
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ConditionsPelvic Floor Prolapse

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pelvic Floor Prolapse
Sponsor
Western Galilee Hospital-Nahariya
Enrollment
140
Locations
2
Primary Endpoint
Symptoms of pelvic floor prolapse
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Women who had surgery for pelvic floor prolapse underwent surgery by anterior Prolift or Posterior prolift at least a year after the surgery.

The data from the charts and from telephone conversations with the patients will be entered to a database. Physical examination data will also be incorporated.

Registry
clinicaltrials.gov
Start Date
February 2009
End Date
June 2013
Last Updated
11 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

menahem neuman

Principal Investigator

Western Galilee Hospital-Nahariya

Eligibility Criteria

Inclusion Criteria

  • •Women who underwent surgery by anterior Prolift or posterior Prolift for pelvic floor prolapse

Exclusion Criteria

  • •Women who did not have surgery by Prolift for pelvic floor prolapse

Outcomes

Primary Outcomes

Symptoms of pelvic floor prolapse

Time Frame: One year after surgery

We will question the women if they have a feeling of a mass protruding through the labia. Physical examination data will also be incorporated.

Study Sites (2)

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