10
Participants
Start Date
May 31, 2014
Primary Completion Date
August 31, 2014
Study Completion Date
August 31, 2014
Evaluation of propofol effect
"The study will make in two stages:~STAGE I: All volunteers will receive propofol infusion with the first model randomly chosen (Schnider or Cortinez) using TCI device, and the initial effect-site target concentration of propofol will be 3 ug/ml for 20 minutes."
Evaluation of propofol effect
STAGE II: 72 hours after stage I . All volunteers will receive propofol infusion with the first model randomly chosen (Schnider or Cortinez) using TCI devices, and the initial effect-site target concentration of propofol will be 3 ug/ml for 20 minutes.
Clinica Avila, Caracas
Collaborators (1)
Medtronic - MITG
INDUSTRY
Tiva Group
OTHER