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Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

This study has been completed.
Information provided by (Responsible Party):
menahem neuman, Western Galilee Hospital-Nahariya Identifier:
First received: June 29, 2011
Last updated: July 2, 2014
Last verified: July 2011

Women who had surgery for pelvic floor prolapse underwent surgery by anterior Prolift or Posterior prolift at least a year after the surgery.

The data from the charts and from telephone conversations with the patients will be entered to a database. Physical examination data will also be incorporated.

Pelvic Floor Prolapse

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective

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

Primary Outcome Measures:
  • Symptoms of pelvic floor prolapse [ Time Frame: One year after surgery ]
    We will question the women if they have a feeling of a mass protruding through the labia. Physical examination data will also be incorporated.

Enrollment: 140
Study Start Date: February 2009
Study Completion Date: June 2013
Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)

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

Inclusion Criteria:

  • Women who underwent surgery by anterior Prolift or posterior Prolift for pelvic floor prolapse

Exclusion Criteria:

  • Women who did not have surgery by Prolift for pelvic floor prolapse
  Contacts and Locations
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Please refer to this study by its identifier: NCT01392417

Department of Obstetrics and Gynecology, Western Galilee Hospital
Nahariya, Israel
Clinics of Dr Neuman
Tel Aviv, Israel
Sponsors and Collaborators
Western Galilee Hospital-Nahariya
  More Information

Responsible Party: menahem neuman, Principal Investigator, Western Galilee Hospital-Nahariya Identifier: NCT01392417     History of Changes
Other Study ID Numbers: 920090043
Study First Received: June 29, 2011
Last Updated: July 2, 2014

Additional relevant MeSH terms:
Pathological Conditions, Anatomical processed this record on May 25, 2017