Intestinal Perforation in Patients Receiving an Orthtopic Liver Transplantation in the Montpellier University Hospital
NCT ID: NCT04180735
Last Updated: 2019-11-29
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
60 participants
OBSERVATIONAL
2019-09-30
2019-10-30
Brief Summary
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The aim of the study is to evaluate the risk factors of intestinal perforations using a retrospective study scheme.
Detailed Description
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The aim of the study is to evaluate the risk factors of intestinal perforations using a retrospective study scheme. Previous studies have shown a possible implication of drugs or medical history or intraoperative complications. The investigators aim to describe the other possible risk factors (such as portal vein clampage) and the type of surgery done after the diagnosis and its impact on survival as well.
Conditions
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Keywords
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Perforation
Perforation
Liver transplantation
Liver transplantation
No perforation
No perforation
Liver transplantation
Liver transplantation
Interventions
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Liver transplantation
Liver transplantation
Eligibility Criteria
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Inclusion Criteria
* for the group Perforation: patients having during the follow-up a complication such as intestinal perforation. The complete list uses the ICD-10 codes for intestinal perforation, esophageal perforation, duodenal perforation etc.
18 Years
65 Years
ALL
No
Sponsors
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Université Montpellier
OTHER
University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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Fabrizio PANARO, PhD
Role: STUDY_DIRECTOR
UH MONTPELLIER
Locations
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Uh Montpellier
Montpellier, , France
Countries
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Other Identifiers
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RECHMPL19_0362
Identifier Type: -
Identifier Source: org_study_id