Developing Anesthesia as Post Traumatic Stress Disorder (PTSD) Therapy
NCT01736020 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 293
Last updated 2016-10-13
Summary
This preclinical phase 1 development study in healthy volunteers seeks to identify if low doses of commonly used non-triggering anesthetic agents might have clinical utility for modulating emotional memory processing and to understand the nature of the brain mechanisms of drug action. Optimally, a drug, dose and brain mechanism of action will be identified that will form the foundation for future use in clinical studies of patients with PTSD.
Conditions
- Healthy
Interventions
- DRUG
-
Dexmedetomidine
A low dose of dexmedetomidine is used during scanning after dose piloting outside the scanner for memory effects and tolerability.
- DRUG
-
Propofol
A low dose of propofol is used during scanning after dose piloting outside the scanner for memory effects and tolerability.
- DRUG
-
A low dose of ketamine is used during scanning after dose piloting outside the scanner for memory effects and tolerability.
- DRUG
-
Nitrous Oxide
A low dose of nitrous oxide is used during scanning after dose piloting outside the scanner for memory effects and tolerability.
- DRUG
-
Placebo
Sponsors & Collaborators
-
National Institute of Mental Health (NIMH)
collaborator NIH -
University of California, Irvine
collaborator OTHER -
Southern California Institute for Research and Education
lead OTHER
Principal Investigators
-
Michael T Alkire, MD · University of California, Irvine and Long Beach VA Medical Center
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 35 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2009-09-30
- Primary Completion
- 2017-04-30
- Completion
- 2017-04-30
Countries
- United States
Study Locations
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