Prolift Versus IVS for Pelvic Floor Prolapse

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01383291
Recruitment Status : Withdrawn
First Posted : June 28, 2011
Last Update Posted : June 20, 2014
Information provided by:
Western Galilee Hospital-Nahariya

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
Pelvic Floor Prolapse

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 : February 2009
Estimated Primary Completion Date : January 2013
Estimated Study Completion Date : June 2013

Pelvic floor prolapse
Those who underwent prolift and those who underwent IVS

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years to 95 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Women with pelvic floor prolapse

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01383291

Department of Obstetrics and Gynecology, Western Galilee Hospital
Nahariya, Israel
Clinics of Dr Neuman
Rishon Lezion, Israel
Sponsors and Collaborators
Western Galilee Hospital-Nahariya

Responsible Party: Dr. Menahem Neuman, Western Galilee Hospital and vaious clinics Identifier: NCT01383291     History of Changes
Other Study ID Numbers: 920090041
First Posted: June 28, 2011    Key Record Dates
Last Update Posted: June 20, 2014
Last Verified: June 2014

Keywords provided by Western Galilee Hospital-Nahariya:
pelvic floor prolapse

Additional relevant MeSH terms:
Pathological Conditions, Anatomical