Study Type
Interventional - Procedure
The LIMIT trial will evaluate safety and efficacy of a common, lower INR target range (1.5 to 2.5) in patients with bileaflet aortic mechanical valves.
LIMIT-LESS, which is an imaging and cognitive sub-study of the LIMIT trial, will explore the association between covert cerebrovascular disease and cognitive measures with different INR targets in participants with bileaflet aortic mechanical valves.
LIMIT Slides - Download PDFInterventional - Procedure
Randomized, open-label, blinded end-point (PROBE), multicenter
20
50
2625
2019 - 2027
PHRI
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