The main objective if to evaluate the sparing effect of dexmedetomidine on the doses of propofol and remifentanil.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
66
Same volume as in the dexmedetomidine group
1 mcg/kg administered in 10 minutes followed by a continuous infusion of 0,5 mcg/kg/hr
Hôpital Foch
Suresnes, France
administered doses of propofol and of remifentanil during anesthesia
Time frame: end of anesthesia
delay before recovery
Time frame: at the end of anesthesia
hemodynamic abnormalities requiring a treatment
Time frame: end of anesthesia
postoperative morphine requirement
Time frame: Third post-anesthetic hour
explicit memorisation
Time frame: Second postoperative day
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