Status:

COMPLETED

Evaluating Ketamine and Psychological Sequelae

Lead Sponsor:

Defense and Veterans Center for Integrative Pain Management

Conditions:

Pain, Ketamine Infusion, Psychologic Sequelae

Eligibility:

All Genders

18+ years

Brief Summary

The purpose of this study is to examine the relationship between the use of intravenous infusion of sub-anesthetic dosages of ketamine given for pain to combat casualties and emerging symptoms of Post...

Detailed Description

The purpose of this study is to examine the relationship between the use of intravenous infusion of sub-anesthetic dosages of ketamine given for pain to combat casualties and emerging symptoms of Post...

Eligibility Criteria

Inclusion

  • Group I. Ketamine Group
  • Active duty military service member injured in theater and treated at WRAMC or at WRNMMC
  • 18 years of age or older
  • Completed the PBBHA or PDHAT initial and follow up assessment post aerovac from theater
  • Received ketamine infusion to treat pain after aero-evacuation for inpatient medical care between Sep 2005 and June 2014
  • Received ketamine before completion of the PDHAT or PDBHA follow-up assessment
  • ISS scores are available for each individual
  • Group II. Non-Ketamine Comparison Group
  • Active duty military service member injured in theater and treated at WRAMC or at WRNMMC
  • 18 years of age or older
  • Completed the PBBHA or PDHAT initial and follow up assessment post aerovac from theater
  • Did not receive ketamine treatment for pain after aero-evacuation for inpatient medical care before follow-up
  • ISS are available for each individual
  • Patient will have ISS scores similar to a Ketamine Group patient and a similar timing of injury to the same Ketamine Group patient.

Exclusion

  • Not treated by WRNMMC/WRAMC hospital staff between Sep 2005 and June 2014
  • Not active duty, activated National Guard, or activated Reserve service members
  • Younger than 18 years of age
  • Did not complete the PDBHA or PDHAT initial and follow-up assessments
  • ISS scores are not available

Key Trial Info

Start Date :

December 1 2014

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 13 2017

Estimated Enrollment :

159 Patients enrolled

Trial Details

Trial ID

NCT04053400

Start Date

December 1 2014

End Date

September 13 2017

Last Update

August 12 2019

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Walter Reed National Military Medical Center

Bethesda, Maryland, United States, 20889