CompletedN/Aketamine

Evaluating Ketamine and Psychological Sequelae

Sponsored by Defense and Veterans Center for Integrative Pain Management

NCT ID
NCT04053400
Target Enrollment
159 participants
Start Date
2014-12
Est. Completion
2017-09-13

About This Study

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-Traumatic Stress Disorder (PTSD), depression, anxiety, sleep disruption, and risk of alcohol abuse as identified with behavioral health screening tools. Although ketamine has gained popularity as an analgesic agent, literature related to its psychological impact is sparse.

Conditions Studied

Pain, Ketamine Infusion, Psychologic Sequelae

Interventions

  • Ketamine

Eligibility

Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

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 Criteria:

* 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

Study Locations (1)

Walter Reed National Military Medical Center
Bethesda, Maryland, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source