Dexmedetomidine Use in Infants Undergoing Cooling Due to Neonatal Encephalopathy (DICE Trial)

Last updated: April 8, 2025
Sponsor: University of Utah
Overall Status: Active - Not Recruiting

Phase

2

Condition

Pain

Neurologic Disorders

Stroke

Treatment

Dexmedetomidine Hydrochloride

Morphine Sulfate

Clinical Study ID

NCT04772222
136561
  • Ages < 24
  • All Genders

Study Summary

Management of neonatal pain and sedation often includes opioid therapy. A growing body of evidence suggests long-term harm associated with neonatal opioid exposure. Providing optimal sedation while neonates are undergoing therapeutic hypothermia (TH) may be beneficial but also presents therapeutic challenges. While there is evidence from animal models of brain injury and clinical trials in adults to support the safety and neuroprotective properties of dexmedetomidine (DMT), there are no published large clinical trials demonstrating safety and efficacy of DMT use in neonates with hypoxic-ischemic encephalopathy (HIE) during treatment with TH. This study is innovative in proposing a Phase II, 2-arm trial providing the opportunity to evaluate the use of DMT as compared to the use of morphine for sedation and pain management for babies undergoing TH. We propose to confirm optimal DMT dosing by collecting opportunistic pharmacokinetics (PK) data and determine safety of DMT in this population. These data will inform a larger phase III efficacy trial.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Neonates ≥36 weeks' gestational age diagnosed with moderate-to-severe neonatalencephalopathy and treated with TH (target temperature 33.5°C) for a plannedduration of 72 h.

  • Infants requiring sedation and/or treatment to prevent shivering during TH asassessed by the Neonatal Pain, Agitation, and Sedation Scale (N-PASS) scores and amodified Bedside Shivering Assessment Scale.

  • Informed consent document approved by the Institutional Review Board (IRB) obtainedprior to randomization

Exclusion

Exclusion Criteria:

  • Known chromosomal anomalies

  • Cyanotic congenital heart defects

  • Redirection of care being considered because of moribund condition, or a decisionmade to withhold full support

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: Dexmedetomidine Hydrochloride
Phase: 2
Study Start date:
June 20, 2022
Estimated Completion Date:
December 31, 2025

Connect with a study center

  • Intermountain Medical Center

    Murray, Utah 84107
    United States

    Site Not Available

  • McKay-Dee Hospital

    Ogden, Utah 84403
    United States

    Site Not Available

  • Utah Valley Hospital

    Provo, Utah 84604
    United States

    Site Not Available

  • Primary Children's Hospital

    Salt Lake City, Utah 84113
    United States

    Site Not Available

  • University of Utah Health

    Salt Lake City, Utah 84132
    United States

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.