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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT01383291
Study type Observational
Source Western Galilee Hospital-Nahariya
Contact
Status Withdrawn
Phase N/A
Start date February 2009
Completion date June 2013

See also
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Completed NCT02680145 - Prediction of Postsurgical Symptomatic Outcomes With Preoperative Pessary Use N/A
Recruiting NCT04547816 - Efficacy of Conservative Treatment of Functional Defecatory Disorders in Females With Pelvic Organ Prolapse Phase 3
Completed NCT03421457 - Laparoscopic Lateral Suspension With Mesh & Sacrocervicopexy for the Treatment of Uterine Prolapse N/A
Completed NCT01392417 - Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse N/A
Withdrawn NCT01387685 - Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh N/A