Scientists collect brain data to create safer pressure monitors
NCT ID NCT04548596
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study gathered brain monitoring data from 162 patients with serious brain injuries, such as traumatic brain injury or stroke. Using a noninvasive ultrasound device, researchers recorded blood flow signals to build a database. The goal is to develop algorithms that could one day measure brain pressure without surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a noninvasive way to measure brain pressure, reducing the need for risky surgical monitors.
- What could go wrong
- This is an early data-collection study, not a treatment trial. The algorithms may not work in real-world settings or may take years to develop.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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162 people
The number who actually took part.
- Started
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Sep 2014
- Finished
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Apr 2025
- 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
The investigators aim to collect multimodality high-resolution physiological signals from brain injured patients: traumatic brain injury, subarachnoid and intracerebral hemorrhage, liver failure, and ischemic stroke.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: 1. Male or female subjects 18 years of age and older 2. Subjects who have an ICP Monitoring device Exclusion Criteria: 1. Unstable medical illness such as recordings might interfere with medical care. 2. Subjects that don't have a viable temporal window to insonate the MCA. 3. Subjects that have skull fractures that the attending or study investigators believe participation would add clinical risk to the subject.
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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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Emory University
Atlanta, Georgia, 30322, United States
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UC Davis
Davis, California, 95616, United States
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University of California San Francisco
San Francisco, California, 94143, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next
- Can a web program rebuild memory after brain injury?
- Two ways to catch a hidden heart rhythm after stroke
- Can brainwave and blood flow data forecast who wakes after a severe brain injury?
- Blood test may reveal who recovers after a stroke