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NCT01392417 Clinical Trial

Anterior Prolift Versus Posterior Prolift for Pelvic Floor Prolapse

Pelvic Floor Prolapse Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01392417
Other study ID # 920090043
Secondary ID
Status Completed
Phase N/A
First received June 29, 2011
Last updated July 2, 2014
Start date February 2009
Est. completion date June 2013

Study information
Verified date July 2011
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 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.

Recruitment information / eligibility
Status Completed
Enrollment 140
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 underwent surgery by anterior Prolift or posterior Prolift for pelvic floor prolapse

Exclusion Criteria:

- Women who did not have surgery by Prolift 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 Tel Aviv

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

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Symptoms of pelvic floor prolapse We will question the women if they have a feeling of a mass protruding through the labia. Physical examination data will also be incorporated. One year after surgery No
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 NCT01383291 - Prolift Versus IVS for Pelvic Floor Prolapse N/A
Withdrawn NCT01387685 - Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh N/A