Cohort Study of Bowel Function Following Robotic-assisted Laparoscopic Sacrocolpopexy
NCT ID: NCT01618292
Last Updated: 2014-01-28
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
393 participants
OBSERVATIONAL
2007-01-31
2012-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Robotic-assisted sacrocolpopexy patients
Patients who underwent robotic-assisted laparoscopic sacrocolpopexy between January 2007 and August 2011.
Robotic sacral colpopexy
Patients who underwent robotic assisted sacral colpopexy for the treatment of pelvic organ prolapse
Interventions
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Robotic sacral colpopexy
Patients who underwent robotic assisted sacral colpopexy for the treatment of pelvic organ prolapse
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
FEMALE
No
Sponsors
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Atlantic Health System
OTHER
Responsible Party
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Jennifer Pagnillo
Patrick Culligan, MD
Principal Investigators
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Patrick Culligan, MD
Role: PRINCIPAL_INVESTIGATOR
Atlantic Health System
Locations
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Atlantic Health System
Morristown, New Jersey, United States
Countries
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Other Identifiers
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R11-08-011
Identifier Type: -
Identifier Source: org_study_id
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