NCT07198711
Induction of Dreaming With EEG and Anesthesia in Healthy Adults
Enrolling by Invitation
PHASE1Ages 18–70InterventionalBasic scienceStanford UniversityInvestigator-initiated
~15 participants
Updated 2026-06-22 on ClinicalTrials.gov
What's tested:Propofol - Emergence-from-LOR ProtocolPropofol - Light Sedation Protocol
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Protocol-concordant experiential report
Measured over Assessed within 5 minutes of return of responsiveness (LOR protocol) or within 5 minutes of session end (light-sedation protocol).
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Study leadership
- Dr. Boris D Heifets, MD, PhD · PRINCIPAL_INVESTIGATOR · Stanford University
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Protocol-concordant experiential reportAssessed within 5 minutes of return of responsiveness (LOR protocol) or within 5 minutes of session end (light-sedation protocol).
Presence vs absence of an experiential report elicited via a structured interview (modified Brice). "Protocol-concordant" is defined as: LOR protocol-success = any dream report upon emergence; Light-sedation (no-LOR) protocol-success = any experiential report that is not a dream (e.g., imagery, sounds, thoughts, bodily sensations, hypnagogic-like experiences) while the participant remained behaviorally responsive.