RecruitingBrain Injuries, Traumatic
Automated Robotic TCD in Traumatic Brain Injury
Eligible age
18+ yrs
Accepts
All genders
Locations
3 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
This study's objective is to determine the safety, feasibility and efficacy of prolonged automated robotic TCD monitoring in critically ill patients with severe TBI across multiple clinical sites with varying levels of TCD availability and experience
Sponsor: Virginia Commonwealth University
You may qualify if…
- ✓ Adults ≥18
- ✓ Blunt TBI with Glasgow Coma Score (GCS) ≤8
- ✓ Injury within 72 hours
- ✓ Adequate TCD windows
- ✓ Ability to obtain informed consent from a Legally Authorized Representative (LAR)
You may not qualify if…
- ✕ Catastrophic brain injury with grim prognosis (e.g.: GCS 3 with bilateral mid-position pupil)
- ✕ C- spine fracture with evidence of spinal cord injury
- ✕ Severe skull or scalp injury precluding device placement
- ✕ Planned decompressive hemicraniectomy
- ✕ Continuous fever for \>6 hours at the time of enrollment (despite treatment)
- ✕ Lack of TCD window
Where it's recruiting
Source: ClinicalTrials.gov · NCT05848297 · last updated 2026-06-03