Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01387685

Enrollment

Registered

2011-07-04

Start date

2009-02-28

Completion date

2013-01-31

Last updated

2014-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Floor Prolapse

Brief 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.

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 95 Years

Healthy volunteers

Inclusion criteria

* Women who underwent surgery for pelvic floor prolapse

Exclusion criteria

* Women who did not have surgery for pelvic floor prolapse.

Design outcomes

Primary

Measure	Time frame
Satisfaction with study outcome	six to twelve months after surgery

Secondary

Measure	Time frame
Side effects of the surgery: pain, vaginal erosion by tape, bleeding	Within six to twelve months after study

Countries

Israel

Outcome results