Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh

Status Withdrawn

Clinical Trial Summary

Women with pelvic floor prolapse who underwent surgery with mesh will be enrolled. The investigators will compare data from the chart, telephone interviews and physical examinations between those who underwent mesh placement to those who underwent placement of PIVS.

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01387685
Study type	Observational
Source	Western Galilee Hospital-Nahariya
Contact
Status	Withdrawn
Phase	N/A
Start date	February 2009
Completion date	January 2013

View Details

See also
Status	Clinical Trial	Phase
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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Withdrawn	`NCT01383291` - Prolift Versus IVS for Pelvic Floor Prolapse	N/A
Completed	`NCT01392417` - Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse	N/A