Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01383291

Prolift Versus IVS for Pelvic Floor Prolapse

Postoperative Comparison Between Posterior Prolift Mesh Placement and Posterior IVS Sling Placement

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Western Galilee Hospital-Nahariya · Other Government
Sex
Female
Age
18 Years – 95 Years
Healthy volunteers
Not accepted

Summary

* 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.

Conditions

Timeline

Start date
2009-02-01
Primary completion
2013-01-01
Completion
2013-06-01
First posted
2011-06-28
Last updated
2014-06-20

Locations

2 sites across 1 country: Israel

Source: ClinicalTrials.gov record NCT01383291. Inclusion in this directory is not an endorsement.

Prolift Versus IVS for Pelvic Floor Prolapse (NCT01383291) · Clinical Trials Directory