Scientists test smarter brain monitoring for injured kids
NCT ID NCT04242602
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 29 children with brain injuries to test two new methods for checking how well the brain controls its own blood flow. The goal was to see if these methods could help doctors better understand and treat brain injuries. The study did not test a treatment, but aimed to improve monitoring techniques.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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29 people
The number who actually took part.
- Started
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Nov 2018
- Finished
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Sep 2020
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Children 1-18 years of age with acute TBI admitted to the pediatric intensive care unit.
- Ages
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28 days to 18 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Ages 28 days-18 years admitted to the PICU at Children's Medical Center Dallas * Acute presentation (\< 24 hour) onset of neurologic injury * Acute neurologic injury can be due to any of the following mechanisms: * Severe accidental or abusive traumatic brain injury * Severe encephalopathy secondary to cardiac arrest * Spontaneous intracranial hemorrhage * Status epilepticus * Stroke * Presence of or pending placement of invasive indwelling arterial line for stand medical care * Any patient with an ICP monitor placed as standard of care Exclusion Criteria: * Patients without an arterial line placed as standard of care * Patients unable to cooperate with wearing a TCD headpiece device * Expected death within 24-48 hours * Inability to place NIRS probes or insonate TCD signal due to massive facial or cranial injury * Receiving an inhalational anesthetic agent * Hemoglobinopathy, myoglobinemia or and hyperbilirubinemia (due to inaccurate NIRS readings)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Children's Medical Center
Dallas, Texas, 75390, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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