A Large Multi-Center Database of Women Who Have Had and Are Going to Have Surgical Correction of Their Pelvic Organ Prolapse Using the Gynecare Prolift System

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01134003

Enrollment

Unknown

Registered

2010-05-31

Start date

2008-01-31

Completion date

2009-12-31

Last updated

2010-05-31

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

Conditions

Pelvic Organ Prolapse

Keywords

Gynecare Prolift, Pelvic organ prolapse, forming a large database of women who have recieve Gynecare prolift system

Brief summary

retrospective and prospective data collection for a database. Patients will have had or are going to have a repair of their pelvic organ prolapse using the Gynecare mesh Prolift System

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Inclusion criteria

* women recieving surgery for their pelvic organ prolapse using the Gynecare mesh kit called Prolift

Exclusion criteria

* none

Countries

United States

Outcome results