Prolift Versus IVS for Pelvic Floor Prolapse

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by:
Western Galilee Hospital-Nahariya
ClinicalTrials.gov Identifier:
NCT01383291
First received: June 26, 2011
Last updated: June 19, 2014
Last verified: June 2014
  Purpose
  • 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
Pelvic Floor Prolapse

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: Postoperative Comparison Between Posterior Prolift Mesh Placement and Posterior IVS Sling Placement

Further study details as provided by Western Galilee Hospital-Nahariya:

Enrollment: 0
Study Start Date: February 2009
Estimated Study Completion Date: June 2013
Estimated Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts
Pelvic floor prolapse
Those who underwent prolift and those who underwent IVS

  Eligibility

Ages Eligible for Study:   18 Years to 95 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Women with pelvic floor prolapse

Criteria

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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01383291

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

No publications provided

Responsible Party: Dr. Menahem Neuman, Western Galilee Hospital and vaious clinics
ClinicalTrials.gov Identifier: NCT01383291     History of Changes
Other Study ID Numbers: 920090041
Study First Received: June 26, 2011
Last Updated: June 19, 2014
Health Authority: Israel: Ministry of Health

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

Additional relevant MeSH terms:
Prolapse
Pathological Conditions, Anatomical

ClinicalTrials.gov processed this record on October 23, 2014