Dexmedetomidine Pharmacokinetics in Neonates During Therapeutic Hypothermia
Public ClinicalTrials.gov record NCT02529202. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Dexmedetomidine Use During Therapeutic Hypothermia Treatment for Neonates With Hypoxic-ischemic Encephalopathy: The Cool DEX Study
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The goal of this proposal is to profile the pharmacokinetics of dexmedetomidine in newborns ≥36 weeks post-menstrual age during therapeutic hypothermia for hypoxic-ischemic encephalopathy.
Study identification
- NCT ID
- NCT02529202
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Early Phase 1
- Enrollment
- 7 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 1 Hour to 1 Day
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Feb 29, 2016
- Primary completion
- Oct 31, 2016
- Completion
- Dec 31, 2016
- Last update posted
- Jan 11, 2017
2016 – 2017
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Seattle Children's Hospital | Seattle | Washington | 98015 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Recently updated Hypoxic-ischemic Encephalopathy trials
Other public records listing Hypoxic-ischemic Encephalopathy. Sorted by last update posted; newest first. Not a recommendation.
- NCT07628829: Neonatal Neurological Observation With Video AI Recruiting
- NCT05610085: A Dose Escalation Study of Levetiracetam in the Treatment of Neonatal Seizures Recruiting
- NCT05971446: Healthy Little Eyes Recruiting
- NCT06195345: Individual Cerebral Hemodynamic Oxygenation Relationships (ICHOR 1) Recruiting
- NCT05778188: A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of RLS-0071 in Newborns With Moderate or Severe Hypoxic-Ischemic Encephalopathy Undergoing Therapeutic Hypothermia Recruiting
- NCT06448780: Dose Optimization of Caffeine for HIE Recruiting
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02529202, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jan 11, 2017 · Synced Sep 10, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02529202 live on ClinicalTrials.gov.