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Prolift Versus IVS for Pelvic Floor Prolapse

Sponsor
Western Galilee Hospital-Nahariya (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01383291
Collaborator
(none)
0
Enrollment
2
Locations
51.9
Duration (Months)
0
Patients Per Site
0
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

  • Women who underwent mesh or sling procedures to correct pelvic organ prolapse will be enrolled.

  • Their data will be collected from the files.

  • Comparison between two groups will be carried our: Those who underwent a posterior IVS and those who underwent posterior prolift procedure.

  • The data will be obtained by questionaires by a telephone interview by a physician who did not participate in the surgery.

  • Follow-up physical examination data will also be obtained.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    0 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Official Title:
    Postoperative Comparison Between Posterior Prolift Mesh Placement and Posterior IVS Sling Placement
    Study Start Date :
    Feb 1, 2009
    Anticipated Primary Completion Date :
    Jan 1, 2013
    Anticipated Study Completion Date :
    Jun 1, 2013

    Arms and Interventions

    Arm Intervention/Treatment
    Pelvic floor prolapse

    Those who underwent prolift and those who underwent IVS

    Outcome Measures

    Primary Outcome Measures

      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 previously underwent surgery for pelvic floor prolapse at least a year before
      Exclusion Criteria:
      • Women who did not have surgery 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 Rishon Lezion Israel

      Sponsors and Collaborators

      • Western Galilee Hospital-Nahariya

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01383291
      Other Study ID Numbers:
      • 920090041
      First Posted:
      Jun 28, 2011
      Last Update Posted:
      Jun 20, 2014
      Last Verified:
      Jun 1, 2014
      Keywords provided by , ,
      pelvic floor prolapse
      prolift
      IVS
      Surgery
      Additional relevant MeSH terms:
      Prolapse

      Study Results

      No Results Posted as of Jun 20, 2014