A Study to Assess the Efficacy and Safety of Fospropofol Disodium
Status:
Completed
Trial end date:
2011-01-01
Target enrollment:
Participant gender:
Summary
The aim of this study was to evaluate the pharmacodynamics, safety, and tolerability of
Fospropofol disodium up to a dose producing maximal hypnotic effect as defined by
electroencephalogramderived assessment (Bispectral Index [BIS]) and to compare the dynamic
properties of PropofolF to those of Propofol.