DOAC in Patients with Child a or B Liver Cirrhosis

Recruiting Phase 2 Interventional Study
Liver Cirrhosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Other
Participants needed
40 (estimated)
Sponsor
Centre Hospitalier Universitaire Vaudois · Other
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About This Trial
The goal of this clinical trial is to investigate pharmacokinetics and pharmacodynamics of direct oral anticoagulant drugs (DOAC), specifically apixaban and edoxaban, in patients with Child A or B liver cirrhosis (LC). The primary objective of this study is to verify the ability of apixaban and edoxaban to decrease in vivo thrombin generation in LC patients. Participants will be randomly assigned…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18 years or older * Patient with previously diagnosed liver cirrhosis Child A or B * Written informed consent Exclusion Criteria: * Pregnancy * Oesophageal varices with grade superior to 1 or with red signs * Active ulcer disease of the gastrointestinal tract * History o…
Contacts

Lorenzo Alberio, Prof Dr. med

0041213140171

lorenzo.alberio@chuv.ch

CONTACT