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
51 participants
OBSERVATIONAL
2020-11-01
2022-07-15
Brief Summary
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The investigators wish to conduct an observational multi-center study with epidemiologic aims, including all patients admitted for AP and with a diagnosis of portosplenomesenteric vein thrombosis. The aim of this study is to evaluate the therapeutic management of these patients, the efficacy and safety of anticoagulant treatment for the treatment of Portosplenomesenteric vein thrombosis, and their outcomes.
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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observational study
patients admitted for AP with portosplenomesenteric vein thrombosis.
Eligibility Criteria
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Inclusion Criteria
* AND a diagnosis on CT injected with portal time of portosplenomesenteric vein thrombosis or laminated veins (without passage of blood flow through the vessel but without visible intraluminal thrombus) will be included.
Exclusion Criteria
* Refusal to participate in research
* Pregnancy
18 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Principal Investigators
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GARRET Charlotte, MD
Role: PRINCIPAL_INVESTIGATOR
University hospital of Nantes
Locations
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CHU de Nantes
Nantes, , France
Countries
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Other Identifiers
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MR_PATHRO
Identifier Type: -
Identifier Source: org_study_id
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