Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
PTSD
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Open label pilot studyMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 70 years
Gender
Both males and females

Description

Current treatments for PTSD do not work for a significant proportion of individuals with PTSD, or work only partially, leaving persistent and disabling residual symptoms. The research team has led the development of ketamine for the treatment of chronic PTSD. After the initial, proof-of-concept rand...

Current treatments for PTSD do not work for a significant proportion of individuals with PTSD, or work only partially, leaving persistent and disabling residual symptoms. The research team has led the development of ketamine for the treatment of chronic PTSD. After the initial, proof-of-concept randomized controlled trial (RCT) of a single ketamine infusion in individuals with chronic PTSD showed promising results, the study team recently completed the first RCT of repeated intravenous ketamine infusions where individuals with chronic PTSD received a course of six ketamine infusions (vs. active placebo midazolam infusions) and demonstrated a rapid and robust improvement in PTSD symptoms. Median time to loss of response, however, occurred a few weeks following the course of infusions, making it imperative to investigate novel approaches aimed at preventing symptom relapse following ketamine treatment. The study team proposes a proof-of-concept, open-label pilot study to evaluate the efficacy of adding an evidence-based, brief and scalable trauma-focused psychotherapy, Written Exposure Therapy (WET), to a course of ketamine infusions in maintaining PTSD symptom improvement over time, in participants with chronic PTSD who respond to initial ketamine infusions. To accomplish this aim, the study team will enroll individuals who meet DSM-5 criteria for chronic PTSD. Patients who show an initial response to four ketamine infusions will be participate in WET (a total of five sessions), and will additionally receive the remaining two ketamine infusions (to complete a total course of six infusions). The primary outcome will be time to loss of response, assessed with the Clinician-Administered PTSD Scale for DSM-5. The study team will also evaluate whether extinction learning ability -assessed with a computerized extinction learning task- predicts maintenance of ketamine response over time, and will explore potential sociodemographic and clinical predictors of longer maintenance of ketamine response. If demonstrated to prolong time to loss of response to ketamine, this novel combined treatment may represent a promising intervention for individuals with chronic PTSD, deserving further study.

Tracking Information

NCT #
NCT04889664
Collaborators
Not Provided
Investigators
Principal Investigator: Adriana Feder, MD Depression and Anxiety Center, Icahn School of Medicine at Mount Sinai Study Director: Oneysha Brown, BA Depression and Anxiety Center, Icahn School of Medicine at Mount Sinai