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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT01392417
Study type Observational
Source Western Galilee Hospital-Nahariya
Contact
Status Completed
Phase N/A
Start date February 2009
Completion date June 2013

See also
  Status Clinical Trial Phase
Completed NCT03387202 - Laparoscopic Lateral Mesh Suspension for Pelvic Organ Prolapse N/A
Not yet recruiting NCT04393194 - The Effect of Intra-vaginal Conjugated Estrogen Cream on Ring Pessary Use for Pelvic Organ Prolapse Phase 4
Recruiting NCT04428320 - The Effect of Preemptive Levator Ani Injections on Pain After Pelvic Reconstructive Surgery N/A
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
Withdrawn NCT01387685 - Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh N/A
Withdrawn NCT01383291 - Prolift Versus IVS for Pelvic Floor Prolapse N/A