Exploring the Safety and Efficacy of Low-dose Ketamine Infusions for Pain Control in Acute Burn Injury
Withdrawn before enrolling · Phase 4
Conditions studied: Pain
In brief
The purpose of this study is to identify the optimal dosing strategy for low-dose ketamine infusions in adult acute burn injury patients when used with usual pain medications.
Key facts
- Study ID
- NCT03095222
- Run by
- University of Kansas Medical Center
- People needed
- 0
- Starts
- 2017-04-01
- Expected to finish
- 2018-05-24
- Last updated by the study team
- 2018-10-31
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Acute burn injury comprising 10-30% of total body surface. Burns severity may include second or third degree burns
- Burn injury must have occurred within 72 hours of enrollment and randomization
- Subjects may be opioid-naïve or opioid non-naïve
- Anticipated stay in the burn unit is greater than 4 days, which is typically the minimum length of stay for patients with this level of burn injury
You may not qualify if…
- Burn injury older than 72 hours
- Acute burn injury comprising >30% total body surface
- Patients who are intubated
- Patients who have contraindication to ketamine administration
Where it is running
- University of Kansas Medical Center — Kansas City, Kansas, United States
Full record on ClinicalTrials.gov
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