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CompletedPhase 2Results posted

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

NCT04772222 · DICE · University of Utah

Closed to entry
Status
Not accepting participants
Phase 2
Phase
50
Target enrolment
5
Study sites
1 US states

What it is testing

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.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Examine Safety Measures in Infants Receiving DMT to Those Receiving Morphine

    Measured over First 96 hours of life

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

24 Hours
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Neonates ≥36 weeks' gestational age diagnosed with moderate-to-severe neonatal encephalopathy and treated with TH (target temperature 33.5°C) for a planned duration of 72 h. * Infants requiring sedation and/or treatment to prevent shivering during TH as assessed by the Neonatal Pain, Agitation, and Sedation Scale (N-PASS) scores and a modified Bedside Shivering Assessment Scale. * Informed consent document approved by the Institutional Review Board (IRB) obtained prior to randomization Exclusion Criteria: * Known chromosomal anomalies * Cyanotic congenital heart defects * Redirection of care being considered because of moribund condition, or a decision made to withhold full support

Where

5 study sites

FacilityCityRegionCountry
Intermountain Medical CenterMurrayUtahUnited States
McKay-Dee HospitalOgdenUtahUnited States
Utah Valley HospitalProvoUtahUnited States
Primary Children's HospitalSalt Lake CityUtahUnited States
University of Utah HealthSalt Lake CityUtahUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

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NCT04772222 on ClinicalTrials.gov →

Last updated in the registry 2026-03-06. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits