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Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh

NCT ID: NCT01387685

Last Updated: 2014-06-20

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

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2009-02-28

Study Completion Date

2013-01-31

Brief Summary

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Women with pelvic floor prolapse who underwent surgery with mesh will be enrolled. The investigators will compare data from the chart, telephone interviews and physical examinations between those who underwent mesh placement to those who underwent placement of PIVS.

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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 for pelvic floor prolapse

Exclusion Criteria

* Women who did not have surgery 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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Western Galilee Hospital and vaious clinics

Locations

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Department of Obstetrics and Gynecology, Western Galilee Hospital

Nahariya, , Israel

Site Status

Dr Neuman clinic

Tel Aviv, , Israel

Site Status

Countries

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Israel

Other Identifiers

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920090042

Identifier Type: -

Identifier Source: org_study_id

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