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NCT07198711

Induction of Dreaming With EEG and Anesthesia in Healthy Adults

Enrolling by Invitation
PHASE1Ages 18–70InterventionalBasic science
Stanford University
~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

Healthy Volunteers

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Healthy Volunteers

NCT07198711

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Stanford University

    Stanford, Californiano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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.