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Treatment Outcomes of Vaginal Prolapse Repair

Sponsor
William Beaumont Hospitals (Other)
Overall Status
Completed
CT.gov ID
NCT00679276
Collaborator
(none)
291
Enrollment
24
Duration (Months)

Study Details

Study Description

Brief Summary

Chart review conducted on all patients having had Prolift surgery since 2005 by Dr. Lary Sirls, Dr. Predeep Nagaraju and Dr. Kenneth Peters at William Beaumont Hospital.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Prolift

Detailed Description

Chart review conducted on all patients having had Prolift surgery since 2005 by Dr. Lary Sirls, Dr. Predeep Nagaraju and Dr. Kenneth Peters at William Beaumont Hospital. Preoperative, intraoperative and post-operative data will be collected from the hospital and physician medical records. A questionnaire will be mailed to patients whose charts have been reviewed to assess urinary and bowel function, satisfaction with treatment and changes in sexual function. Completion of the questionnaire is voluntary.

Study Design

Study Type:
Observational
Actual Enrollment :
291 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Treatment Outcomes of Vaginal Prolapse Repair
Study Start Date :
May 1, 2008
Actual Primary Completion Date :
May 1, 2010
Actual Study Completion Date :
May 1, 2010

Arms and Interventions

Arm Intervention/Treatment
1

Patients having surgical repair of a vaginal prolapse .

Procedure: Prolift
surgical repair of vaginal prolapse

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Women having Prolift repair at William Beaumont Hospital
    Exclusion Criteria:
    • None

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • William Beaumont Hospitals

    Investigators

    • Principal Investigator: Predeep Nagaraju, MD, William Beaumont Hospitals

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00679276
    Other Study ID Numbers:
    • 2008-102
    First Posted:
    May 16, 2008
    Last Update Posted:
    Jun 7, 2010
    Last Verified:
    Jun 1, 2010
    Keywords provided by , ,
    vaginal prolapse
    Additional relevant MeSH terms:
    Uterine Prolapse
    Prolapse

    Study Results

    No Results Posted as of Jun 7, 2010