164
Participants
Start Date
October 31, 2011
Primary Completion Date
August 31, 2012
Study Completion Date
August 31, 2012
Rémifentamil + KETAMINE
All consecutive mechanically ventilated patients admitted in the ICU will be randomized to receive an infusion of 0.15 mg/kg/h of kétamine or placebo. Nurses and physicians will be blinded of the allocation arm. The infusion of ketamine will be stopped as soon as remifentanil will be discontinued by the physician.
ketamine
to evaluate the impact of ketamine associated to an opioid for sedation of mechanically ventilated critically ill patients versus placebo. Sedation will be drive by nurses according to an algorithm. The investigators will evaluate the quantity of opioates used in each arm and the safety of ketamine.
CHU Clermont-Ferrand, Clermont-Ferrand
University Hospital, Clermont-Ferrand
OTHER