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CompletedNCT01392417Updated Jul 3, 2014

Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

An observational study in Pelvic Floor Prolapse, sponsored by Western Galilee Hospital-Nahariya. Completed at 2 sites in Israel. Open to female participants aged 18 Years to 95 Years. Per ClinicalTrials.gov, last updated 2014-07-03.

Sponsored by Western Galilee Hospital-Nahariya · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
140
Ages
18 Years to 95 Years
Sex
Female
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Study summary

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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Conditions studied

  • Pelvic Floor Prolapse

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03

In context

Prolapse

676 studies on the registry are indexed under Prolapse; 79 are open to participants now.

This study's enrollment of 140 is above the median of 126 across 222 observational studies indexed under Prolapse.

Browse Prolapse studies →

Lead sponsor

Western Galilee Hospital-Nahariya is the lead sponsor of 87 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 95 Years
Sexes eligible
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

Exclusion Criteria:

  • Women who did not have surgery by Prolift for pelvic floor prolapse
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Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
140 participants (actual)
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What researchers measure

Primary outcomes

  1. Symptoms of pelvic floor prolapse

    We will question the women if they have a feeling of a mass protruding through the labia. Physical examination data will also be incorporated.

    Time frame: One year after surgery

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Study locations

2 sites
  • Department of Obstetrics and Gynecology, Western Galilee Hospital
    Nahariya, Israel
  • Clinics of Dr Neuman
    Tel Aviv, Israel
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 3, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01392417
Lead sponsor
Western Galilee Hospital-Nahariya
Responsible party
menahem neuman (Principal Investigator, Western Galilee Hospital-Nahariya) — Principal investigator
First posted
Jul 12, 2011
Start date
Feb 2009
Primary completion
Jan 2013
Completion
Jun 2013
Last update
Jul 3, 2014

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2011. You cannot join it, but the record below documents what was studied.

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