Actively Recruiting
Hemodynamic ABI Monitor
Led by University of Chicago · Updated on 2026-03-04
50
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
U
University of Chicago
Lead Sponsor
B
Baxter Healthcare Corporation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this observational study is to explore the relationship of heart function with the course and outcomes after traumatic brain injuries and nontraumatic intracerebral hemorrhage. The goal is to explore association between routinely collected hemodynamic and brain monitoring data. Participants already taking intervention A as part of their regular medical care and the investigators will follow up with participants 6 months after discharging the hospital.
CONDITIONS
Official Title
Hemodynamic ABI Monitor
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Admitted to the University of Chicago Medical Center Neurocritical Care Unit
- Adults between 18 years and 80 years old
- Admitted with traumatic brain injury (blunt or penetrating) or nontraumatic intracerebral hemorrhage
- Post-resuscitation Glasgow Coma Scale (GCS) less than 9
You will not qualify if you...
- Pre-existing heart failure
- Moribund or neurological exam suggesting imminent brain death (bilateral, fixed and dilated pupils) on admission
- Major polytrauma or admitted to the surgical trauma critical care service
- Prisoner
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Chicago
Chicago, Illinois, United States, 60637
Actively Recruiting
Research Team
F
Farima Fakhri, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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