One Year Outcome After Robotic Assisted Laparoscopic Sacral Colpopexy, a Case Series Review
NCT ID: NCT01055860
Last Updated: 2011-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
75 participants
OBSERVATIONAL
2009-02-28
2010-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Robotic sacral colpopexy
Our study population will be women who underwent Robotic assisted laparoscopic sacral colpopexy at the Morristown Memorial Hospital for correction of pelvic organ prolapse using a synthetic polypropylene mesh.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Enrollment in a different study.
21 Years
FEMALE
No
Sponsors
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Atlantic Health System
OTHER
Responsible Party
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Atlantic Health System
Principal Investigators
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Patrick Culligan, MD
Role: PRINCIPAL_INVESTIGATOR
Atlantic Health System
Locations
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Atlantic Health Urogynecology
Morristown, New Jersey, United States
Countries
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Other Identifiers
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R09-02-007
Identifier Type: -
Identifier Source: org_study_id
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