36
Participants
Start Date
May 10, 2024
Primary Completion Date
October 3, 2025
Study Completion Date
October 3, 2025
Functional Magnetic Resonance Imaging (fMRI) with propofol
Three 16-min sessions in wakeful baseline, light sedation, and recovery will be conducted (Fig. 2). Light sedation will be achieved by IV infusion of propofol to achieve effect-site concentrations of 1.0 μg/ml. Infusion rate will be manually controlled. An initial bolus dose (525 µg/kg) and subsequent infusion rate (82 µg/kg/min) for each participant
University of Michigan, Ann Arbor
National Institute of General Medical Sciences (NIGMS)
NIH
University of Michigan
OTHER