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OpenTrials
Completed

NCT Number: NCT01392417

Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

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.

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Key information

Age range

18 year–95 year

Sex eligibility

Female

Study type

Observational

Primary location

Department of Obstetrics and Gynecology, Western Galilee Hospital, Nahariya, Israel

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. 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.

Sponsors and collaborators

Lead sponsor

Western Galilee Hospital-Nahariya

Other Gov

Registry information

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Jul 12, 2011
Registry last updated
Jul 3, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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