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CompletedNCT01889537VRKUpdated Sep 1, 2017

Low Dose Ketamine VR Analgesia During Burn Care Procedure

A Phase 2 interventional study of Virtual Reality in Burn, sponsored by National Institute of General Medical Sciences (NIGMS). Completed at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2017-09-01.

Sponsored by National Institute of General Medical Sciences (NIGMS) · Phase 2, Interventional, and Health services research

Phase
Phase 2
Study type
Interventional
Enrollment
3
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The purpose of the research is to see whether a low dose of ketamine, a medication used to reduce pain, enhances the effectiveness of a virtual reality video game, which is used as a form of distraction from pain during a painful burn care procedure.

Read the detailed description

This study is conducted in a hospital setting. It is a randomized controlled trial comparing the use of virtual reality distraction (VRD) and standard pain medications to the use of VRD, standard pain medications and a single low dose of ketamine as a means to reduce pain during a painful procedure in patients in the hospital.

02

Conditions studied

  • Burn

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Keywords

  • Virtual Reality Ketamine
03

In context

Burns

719 studies on the registry are indexed under Burns; 145 are open to participants now.

This study's enrollment of 3 is below the median of 40 across 524 interventional studies indexed under Burns.

Browse Burns studies →

Lead sponsor

National Institute of General Medical Sciences (NIGMS) is the lead sponsor of 19 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age greater than or equal to 18 years
  • Compliant and able to complete questionnaires
  • No history of psychiatric disorder
  • Not demonstrating delirium, psychosis or any form of Organic Brain Disorder
  • Able to communicate verbally
  • English-speaking
  • IV access already in place

Exclusion criteria

Exclusion Criteria:

  • Age less than 18 years
  • Not capable of indicating pain intensity
  • Not capable of filling out study measures
  • Evidence of traumatic brain injury
  • History of psychiatric disorder
  • Demonstrating delirium, psychosis or any form of Organic Brain Disorder and associated memory problems
  • Unable to communicate orally
  • Receiving prophylaxis for alcohol or drug withdrawal
  • Developmental disability
  • Any face/head/neck injuries that interfere with the use of Virtual Reality equipment
  • Non-English Speaking
  • Extreme susceptibility to motion sickness
  • Seizure history
  • No IV access already in place
05

Study design

Phase
Phase 2
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
3 participants (actual)

Study arms

  • Experimental
    VR during burn care with Ketamine

    Comparing Virtual Reality during burn care with Ketamine

    Behavioral: Virtual Reality

  • Experimental
    VR durin burn care without Ketamine

    Comparing virtual reality during burn care without Ketamine.

    Behavioral: Virtual Reality

Interventions

  • BehavioralVirtual Reality

    The patient will receive virtual reality during a burn care procedure

06

What researchers measure

Primary outcomes

  1. Graphic Rating Scale (GRS) is a questionnaire consists of three subjective pain ratings, one subjective anxiety rating, and one rating of fun using the 0-10.

    Time frame: 1 day (Immediately following burn care )

07

Study locations

1 site
  • Harborview Medical Center
    Seattle, Washington 98104, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 1, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01889537
Lead sponsor
National Institute of General Medical Sciences (NIGMS)
Responsible party
David R. Patterson (PhD. ABPP, Professor, National Institute of General Medical Sciences (NIGMS)) — Principal investigator
First posted
Jun 28, 2013
Start date
Jul 2012
Primary completion
Jun 2015
Completion
Jun 2015
Last update
Sep 1, 2017

Study contacts

David R Patterson, Ph.D.
principal investigator · University of Washington

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

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