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Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01392417
Enrollment
140
Registered
2011-07-12
Start date
2009-02-28
Completion date
2013-06-30
Last updated
2014-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Floor Prolapse

Brief 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.

Interventions

None listed

Sponsors

Western Galilee Hospital-Nahariya
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 95 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Symptoms of pelvic floor prolapseOne year after surgeryWe will question the women if they have a feeling of a mass protruding through the labia. Physical examination data will also be incorporated.

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026