Automated Robotic TCD in Traumatic Brain Injury (ART-TBI)
Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
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
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:
• 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)
Locations
United States
California
University of California, Davis
NOT_YET_RECRUITING
Davis
North Carolina
Wake Forest University
NOT_YET_RECRUITING
Winston-salem
Virginia
Virginia Commonwealth University
RECRUITING
Richmond
Contact Information
Primary
Shraddha Mainali, MD
shraddha.mainali@vcuhealth.org
(804) 828-5269
Backup
Matthew Ridder
matthew.ridder@vcuhealth.org
(804) 828-5269
Time Frame
Start Date: 2025-05-20
Estimated Completion Date: 2026-05
Participants
Target number of participants: 30
Treatments
Prolonged automated TCD
Related Therapeutic Areas
Sponsors
Leads: Virginia Commonwealth University
Collaborators: Wake Forest University, University of California, Davis