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NCT01383291 Clinical Trial

Prolift Versus IVS for Pelvic Floor Prolapse

Pelvic Floor Prolapse Clinical Trial

Official title:
Postoperative Comparison Between Posterior Prolift Mesh Placement and Posterior IVS Sling Placement

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01383291
Other study ID # 920090041
Secondary ID
Status Withdrawn
Phase N/A
First received June 26, 2011
Last updated June 19, 2014
Start date February 2009
Est. completion date June 2013

Study information
Verified date June 2014
Source Western Galilee Hospital-Nahariya
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

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.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date June 2013
Est. primary completion date January 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria:

- Women who previously underwent surgery for pelvic floor prolapse at least a year before

Exclusion Criteria:

- Women who did not have surgery for pelvic floor prolapse

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Department of Obstetrics and Gynecology, Western Galilee Hospital Nahariya
Israel Clinics of Dr Neuman Rishon Lezion

Sponsors (1)
Lead Sponsor Collaborator
Western Galilee Hospital-Nahariya

Country where clinical trial is conducted

Israel, 

See also
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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 NCT01387685 - Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh N/A
Completed NCT01392417 - Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse N/A