Phase 2Recruiting

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

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

Sponsor
Stanford University (Academic or other)
Enrolment
42 planned
Conditions
PTSD; Post-traumatic Stress Disorder
Interventions
Propofol
Ages
adults, older adults
Registry
NCT06577636

Full record on ClinicalTrials.gov

From the registry

The goal of this study is to test whether anesthesia-induced experiences can help alleviate symptoms of PTSD in an (1) open-label trial (Phase I) and (2) single-center double-blind, randomized, active-comparator (dose-controlled) participant-and assessor-blinded Phase 2 clinical trial (Phase II) in a non-surgical setting. Participants will undergo EEG-guided propofol anesthesia during which they will be either (1) receiving a sedation protocol associated with dream experiences upon emergence (Dream Condition), and/or (2) a sedation protocol associated with non-dream experiences (Non-Dream Condition). The investigators will then investigate whether the Dream Condition is associated with a larger reduction in PTSD symptoms than the Non-Dream Condition.

Primary outcomes

  • Clinician-Administered PTSD Scale for DSM-5 (CAPS-5)

History

  1. Study completion expected

  2. Primary completion expected

  3. Last registry update

  4. Started

  5. Registered