RecruitingNCT06966713

Predict Severe Traumatic Brain Injury

Prediction and Prevention of Intracranial Hypertension and Tissue Hypoxia in Severe Traumatic Brain Injury


Sponsor

University of Chicago

Enrollment

120 participants

Start Date

Feb 20, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Severe traumatic brain injury (TBI) is associated with a 20-30% mortality rate and significant disability among most survivors. The Centers for Disease Control and Prevention (CDC) estimate that 2% of the U.S. population lives with disabilities directly attributable to TBI, with annual costs exceeding $76.5 billion. Current treatments are largely ineffective because they are instituted after irreversible damage has already occurred. By the time intracranial pressure (ICP) increases or brain tissue oxygen tension (PbtO2) decreases to harmful levels, it is often too late to reverse or repair the damage. A computerized method has been developed that can predict these injurious events ahead of time, allowing clinicians to intervene before further damage occurs. The goal of this proposal is to test these predictions in real time. The first phase of the project (Year 1) involves setting up the informatics infrastructure, with no patient interaction. In the second phase (Year 2), subjects, through surrogate decision-makers, will be enrolled in an observational study where data on intracranial pressure and brain tissue oxygen tension will be collected, and the prediction algorithm will be tested for accuracy. Clinical management will follow standard care protocols, and no additional interventions will be performed. Approximately 120 individuals will participate in this study at the University of Chicago and Ben Taub General Hospital in Houston. Data collected will include both the electronic medical record and data from bedside intensive care unit monitors. The electronic medical record includes demographic information, injury characteristics, laboratory values, and imaging data, while the intensive care unit monitor provides real-time vital signs such as intracranial pressure, brain tissue oxygen tension, and mean arterial pressure. These data will be securely stored in a research computer database. Efforts will be made to contact subjects or their caretakers at 6 months to follow up on recovery. This research aims to improve patient outcomes by providing predictions of further brain injury, with the potential for future interventions to prevent permanent brain damage.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether advanced brain monitoring tools — which measure pressure inside the skull and oxygen levels in the brain — can better predict recovery and guide treatment decisions in people with severe traumatic brain injury (TBI). **You may be eligible if...** - You are over 18 years old - You have sustained a severe traumatic brain injury (a score of 8 or lower on the Glasgow Coma Scale — a standard assessment of consciousness) - You require brain pressure and/or brain oxygen monitoring as part of your standard ICU care - You can be enrolled while in the ICU **You may NOT be eligible if...** - Your brain injury is so severe that brain death appears imminent (e.g., both pupils are fixed and dilated) - Your neurological exam is unreliable (e.g., due to high alcohol level or seizures) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(2)

University of Chicago

Chicago, Illinois, United States

Baylor college of medicine

Houston, Texas, United States

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NCT06966713


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