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Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

Sponsor
Western Galilee Hospital-Nahariya (Other)
Overall Status
Completed
CT.gov ID
NCT01392417
Collaborator
(none)
140
Enrollment
2
Locations
51.9
Duration (Months)
70
Patients Per Site
1.3
Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    140 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Study Start Date :
    Feb 1, 2009
    Actual Primary Completion Date :
    Jan 1, 2013
    Actual Study Completion Date :
    Jun 1, 2013

    Outcome Measures

    Primary Outcome Measures

    1. Symptoms of pelvic floor prolapse [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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 95 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Obstetrics and Gynecology, Western Galilee Hospital Nahariya Israel
    2 Clinics of Dr Neuman Tel Aviv Israel

    Sponsors and Collaborators

    • Western Galilee Hospital-Nahariya

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    menahem neuman, Principal Investigator, Western Galilee Hospital-Nahariya
    ClinicalTrials.gov Identifier:
    NCT01392417
    Other Study ID Numbers:
    • 920090043
    First Posted:
    Jul 12, 2011
    Last Update Posted:
    Jul 3, 2014
    Last Verified:
    Jul 1, 2011
    Additional relevant MeSH terms:
    Prolapse

    Study Results

    No Results Posted as of Jul 3, 2014