RecruitingPhase 4ketamine

Low-Dose Ketamine Infusion During Burn Wound Care

Sponsored by University of Tennessee

NCT ID
NCT06506565
Target Enrollment
140 participants
Start Date
2024-07-08
Est. Completion
2025-12

About This Study

The current standard of care (SOC) (i.e. fentanyl and midazolam) offers limited efficacy for preventing or relieving pain. Ketamine infusions may provide the benefits of analgesia, minimize adverse events, and reduce opioid use. The purpose of this study is to determine if adding a low dose ketamine infusion during wound care will safely provide pain relief for patients with burn injury.

Conditions Studied

BurnPainDissociationOpioid

Interventions

  • Ketamine
  • 0.9% NaCl

Eligibility

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

* Admitted to burn service with thermal injury

Exclusion Criteria:

* unable/unwilling to consent within 72 hours
* unable to report NRS
* known contraindication to ketamine
* \< than 18 years of age
* pregnant
* incarcerated
* TBSA over 50 %

Study Locations (1)

Regional One Health
Memphis, Tennessee, United States

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

David M Hill, Pharm.D.
CONTACT
1-901-545-7100dhill19@uthsc.edu
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source