70
Participants
Start Date
March 4, 2025
Primary Completion Date
February 1, 2028
Study Completion Date
April 1, 2028
Propofol
Targeted propofol infusion in TRD patients will induce sedation. Dosage of propofol is determined based upon EEG markers and treatment arm.
Electroencephalography (EEG)
EEG will be recorded during propofol infusion and during overnight sleep. Sleep EEG data will be acquired for a minimum of one night prior to the first sedation session, providing a baseline measure. Additional overnight sleep recordings will be performed on day of sedation and subsequent nights.
Brief Behavioral Therapy for Insomnia
Trained staff will provide evaluation and up to 3 follow up appointments of BBTI for all participants. These will be done remotely to assess behavioral approaches to improve overall sleep habits.
RECRUITING
Washington University School of Medicine/Barnes-Jewish Hospital, St Louis
National Institute of Mental Health (NIMH)
NIH
Washington University School of Medicine
OTHER