RecruitingNot Applicable

Hemodynamic ABI Monitor

United States50 participantsStarted 2024-12-06

Plain-language summary

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.

Who can participate

Age range18 Years – 80 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion: Patients who are: * Admitted to the University of Chicago Medical Center Neurocritical Care Unit * Adults between 18 years and 80 * Admitted with Traumatic brain injury blunt and penetrating or nontraumatic intracerebral hemorrhage * post-resuscitation Glasgow Coma Scale (GCS) \<9 Exclusion: Patients who were: * 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

What they're measuring

functional outcomes

Timeframe: 180 days after discharging the hospital

Trial details

NCT IDNCT06725108

SponsorUniversity of Chicago

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-12-06

Contact for this trial

Farima Fakhri, MD

3126102482 farima.fakhri@bsd.uchicago.edu

View on ClinicalTrials.gov More Traumatic Brain Injury (TBI) trials