Cirrhosis Clinical Trial
Official title:
Portal Vein Thrombosis in Cirrhosis: A Cohort Sudy
This study evaluates the supervivence of cirrhotic patients that develop portal vein thrombosis in comparison to cirrhotic patients that do not develop portal vein thrombosis.
Patients newly diagnosed with portal vein thrombosis by imaging tests, that evaluate the
extent and exclude tumoral origin, will be included (informed consent previously signed).
Anticoagulant treatment will be initiated according to clinical guidelines (if there is no
contraindication) first with LMWH (low molecular weight heparin) and later with dicoumarin.
An abdominal CT will be performed to evaluate the extent and exclude tumoral origin; a
gastroscopy to evaluate portal hypertension (and do prophylaxis if required) and
thrombophilia study.
Patients will be followed by imaging and laboratory tests every 6 months; to evaluate the
response to the treatment and detect any cirrhosis complication.
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