This trial intends to evaluate Remimazolam Besylate's availability and safety compared with propofol.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
84
Remimazolam Besylate are used as sedatives for subjects in this arm.
Propofol are used as sedatives for subjects in this arm.
Satisfaction rate of sedation
(number of subjects that meets satisfied RASS score under prescribed dose of sedative agents during study / total number of subjects) ×100%
Time frame: 24 hours since injection of sedatives
Rate of major clinical events
(number of subjects that suffer from major clinical events during study / total number of subjects) ×100%. Major clinical events are defined as cardiac arrest, malignant arrhythmia, new onset of shock, new onset of sepsis and respirate failure unrelated to primary illness.
Time frame: 48 hours since injection of sedatives
incidence of delirium
(subjects with delirium / total number of subjects ×100%) by 12h and 24h after entering ICU
Time frame: 48 hours since injection of sedatives
Time to weaning and extubation
Time to weaning and extubation
Time frame: 48 hours since injection of sedatives
Difficulty of nursing
By Barthel index assessment
Time frame: 48 hours since injection of sedatives
28-days survival
(number of subjects that alive in 28-days since ICU entry/ total number of subjects) ×100%
Time frame: 28 days since injection of sedatives
incidence of rescue therapy in experimental group
(number of subjects that receive rescue therapy in experimental group/ total number of subjects) ×100%
Time frame: 24 hours since injection of sedatives
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