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
Sponsor
The Institute of Pelvic Medicine & Reconstructive Surgery, Allentown, Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT01134003
Collaborator
(none)
1
23
Study Details
Study Description
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
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
|
Study Design
Study Type:
Observational
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
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
Study Start Date
:
Jan 1, 2008
Actual Primary Completion Date
:
Nov 1, 2009
Actual Study Completion Date
:
Dec 1, 2009
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
Female
Inclusion Criteria:
- women recieving surgery for their pelvic organ prolapse using the Gynecare mesh kit called Prolift
Exclusion Criteria:
- none
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Institute for Female Pelvic Medicine and Reconstructive Surgery | Allentown | Pennsylvania | United States | 18103 |
Sponsors and Collaborators
- The Institute of Pelvic Medicine & Reconstructive Surgery, Allentown, Pennsylvania
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT01134003
Other Study ID Numbers:
- SLHN 2007-98
First Posted:
May 31, 2010
Last Update Posted:
May 31, 2010
Last Verified:
May 1, 2010
Keywords provided by ,
,
Additional relevant MeSH terms: