50 brain injury patients help doctors rethink ICU monitoring
NCT ID NCT07285733
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked back at data from 50 patients with severe brain injuries (from trauma or bleeding) who were treated in the ICU. Researchers analyzed brain blood flow, oxygen levels, and scans to understand how treatments affect the brain and body. The goal is to develop more personalized care for future patients.
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
-
50 people
The number who actually took part.
- Started
-
Feb 2010
- Finished
-
Apr 2014
- Lead sponsor
-
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
Primarily admitted to the Antwerp University Hospital
- Ages
-
18 to 70 years
- Sex
-
Anyone
- Healthy volunteers
-
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.
This study is based on the 50 patients recruited for the original study. For TBI: Inclusion Criteria: * male or female patients aged 18 to 70 years, inclusive * sustained head injury within the previous 24 hours * TBI diagnosed by history, clinical examination with a GCS of 12 or less * evidence of TBI confirmed by abnormalities on CT scan * clinical indication to monitor ICP * informed consent is obtained from the patient or from a legally acceptable representative Exclusion Criteria: * life expectancy of less than 24 hours as determined by the investigator * any spinal cord injury * coma suspected to be primarily due to causes other than head injury, such as drug or alcohol overdose * clinically significant or active gastro-intestinal, renal, hepatic, endocrine or CNS disease or chronic condition (e.g.psychiatric disorder) that can be ascertained at the time of admission and could affect functional outcome * respiratory/hemodynamic instability, refractory to treatment and precluding transport for neuroimaging studies * pregnancy * special exclusion criteria for MRI, such as non-removable metals, artificial joints, electronic devices (pacemaker, pumps etc.) * informed consent is obtained from a legally acceptable representative, prior to any study related activity For aneurysmal subarachnoid hemorrhage: Inclusion Criteria: * male or female patients aged 18 to 70 years, inclusive * ruptured aneurysm, demonstrated by CT angiography or DSA * onset of SAH clinical symptoms within the preceding 72 hours * World Federation of Neurosurgery (WFNS) grade III-IV and grade V patients, who improve within 24 hours after ventriculostomy * indication for ICP monitoring or CSF drainage * informed consent is obtained from the patient or a legally acceptable representative Exclusion Criteria: * non-aneurysmal subarachnoid hemorrhage * admission in a clinical state with extremely poor prognosis (e.g. wide, non-reactive pupils for more than 1 hour) * significant coagulation disturbances (thrombocytes \< 80 per mL, partial thromboplastin time \> 45 sec, INR \> 1.5) * cytostatic therapy in patients with malignant disease * pregnancy * special exclusion criteria for MRI, such as non-removable metals, artificial joints, electronic devices (pacemaker, pumps etc.) * respiratory and/or hemodynamic instability precluding
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Subarachnoid aneurysm hemorrhage are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can group wellness classes improve life after brain injury or dementia?
- Can a web program rebuild memory after brain injury?
- Why a simple fall can cause brain bleeding in older adults
- Bedside ultrasound could flag hidden brain injury decline
- Zapping the brain to restore lost vision
- Machine learning may forecast brain decline after head injury