Prolift Versus IVS for Pelvic Floor Prolapse

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2011 by Western Galilee Hospital-Nahariya.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Western Galilee Hospital-Nahariya
ClinicalTrials.gov Identifier:
NCT01383291
First received: June 26, 2011
Last updated: July 23, 2011
Last verified: July 2011
  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:

Estimated Enrollment: 110
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT01383291

Contacts
Contact: Menahem Neuman, MD 0546444033 mneuman@netvision.net.il

Locations
Israel
Department of Obstetrics and Gynecology, Western Galilee Hospital Recruiting
Nahariya, Israel
Sub-Investigator: Jacob Bornstein, MD, MPA         
Sub-Investigator: Vladimir Sosnovsky, MD         
Sub-Investigator: Rene Tendler, MD         
Sub-Investigator: Mohamed Kais, MD         
Clinics of Dr Neuman Recruiting
Rishon Lezion, Israel
Contact: Menahem Neuman, MD         
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: July 23, 2011
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 April 14, 2014