Researchers are studying the safety and efficacy of Dabigatran in the treatment of acute pancreatitis.
Subjects with acute pancreatitis who meet the inclusion and exclusion criteria for the study will be recruited. Subjects will be randomized to receive either Dabigatran 150mg daily for three days or standard treatment. Vital signs, CBC, inflammatory markers and BMP, and bleeding complications will be evaluated daily for the next 7 days of until discharge whichever is sooner.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2
Dabigatran 150mg BID for 3 days
Daily vital signs, lab work and one outpatient clinic visit
Mayo clinic
Jacksonville, Florida, United States
Adverse Events
Number of Reported Adverse Events
Time frame: One year
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