The aim of this study is to validate that an effect compartment concentration for loss of consciousness (LOC) was varied according to different Keo value.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
SINGLE
Enrollment
60
Two TCI devices with different Teo and same Marsh PK model
Two TCI devices with different Teo and same Marsh PK model
Estimated effect-site propofol concentration at loss of consciousness
Time frame: after propofol infusion
Time to loss of consciousness
Time frame: after propofol infusion
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