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RECRUITING
NCT06577636
PHASE2

Induction of Dreaming With EEG and Anesthesia for Post-traumatic Stress Disorder

Sponsor: Stanford University

View on ClinicalTrials.gov

Summary

The goal of this study is to test whether anesthesia-induced dreaming can help alleviate symptoms of PTSD in an (1) open-label trial (Phase I) and (2) double-blind, randomized controlled trial (Phase II) in a non-surgical setting. The investigators predict that inducing and sustaining a dream state prior to emergence from anesthesia will result in reduced symptoms of PTSD. Participants will undergo EEG-guided propofol anesthesia during which they will be either (1) receiving deep sedation leading to loss of responsiveness, designed to elicit dream reports upon emergence (Dream Protocol), and/or (2) light sedation without loss of responsiveness, designed to elicit non-dream experiential reports while responsive (e.g., simple imagery, sounds, thoughts, bodily sensations, hypnagogic-like experiences) (Non-Dream Protocol). The investigators will then investigate whether the deep-sedation Dream Condition is associated with a larger reduction in PTSD symptoms than the light-sedation Non-Dream Condition.

Official title: Efficacy of Anesthesia-induced Dreaming for Post-traumatic Stress Disorder: a Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

42

Start Date

2025-07-21

Completion Date

2026-12

Last Updated

2026-02-24

Healthy Volunteers

No

Interventions

PROCEDURE

Propofol anesthesia

EEG-guided infusion of anesthestetics

Locations (1)

Stanford University

Stanford, California, United States