Is Routine Cholecystectomy Reasonable in All Patients Receiving a Bypass Procedure: a Comparative Cohort Study
NCT ID: NCT01219166
Last Updated: 2010-12-10
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
437 participants
OBSERVATIONAL
2010-12-31
2010-12-31
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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laparoscopic Roux-en-Y-gastric-bypass without cholecystectomy
No interventions assigned to this group
laparoscopic Roux-en-Y-gastric baypass with cholecystectomy
Laparoscopic Cholecystectomy
Laparoscopic Cholecystectomy
Interventions
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Laparoscopic Cholecystectomy
Laparoscopic Cholecystectomy
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* open gastric bypass procedure
* previous bariatric procedure other than gastric banding
* patients lost to follow up
18 Years
ALL
No
Sponsors
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Cantonal Hospital of St. Gallen
OTHER
Responsible Party
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Kantonal Hospital St. Gallen, Department of Visceral Surgery
Principal Investigators
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Martin Thurnheer, MD
Role: PRINCIPAL_INVESTIGATOR
Cantonal Hospital St. Gallen
Locations
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Department of surgery
Sankt Gallen, , Switzerland
Countries
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Other Identifiers
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EKSG10/140/U
Identifier Type: -
Identifier Source: org_study_id