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Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

NCT ID: NCT01392417

Last Updated: 2014-07-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

140 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-02-28

Study Completion Date

2013-06-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Pelvic Floor Prolapse

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

95 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Western Galilee Hospital-Nahariya

OTHER_GOV

Sponsor Role lead

Responsible Party

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menahem neuman

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department of Obstetrics and Gynecology, Western Galilee Hospital

Nahariya, , Israel

Site Status

Clinics of Dr Neuman

Tel Aviv, , Israel

Site Status

Countries

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Israel

Other Identifiers

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920090043

Identifier Type: -

Identifier Source: org_study_id

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