Developing Anesthesia as Post Traumatic Stress Disorder (PTSD) Therapy

NCT01736020 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 293

Last updated 2016-10-13

No results posted yet for this study

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

Ketamine

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

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01736020 on ClinicalTrials.gov