SENSE monitor for intracranial hemorrhage - Clinical Trial

What is the Purpose of this Study?

We are doing this study to determine whether the SENSE device can help determine whether someone with bleeding in the brain is continuing to have more bleeding.

What is the Condition Being Studied?

Brain Injury

Who Can Participate in the Study?

Adults ages 18 and older who have bleeding in the brain due to stroke or injury.

Age Group
Adults

What is Involved?

If you choose to join this study, you will:
- Have a CT scan of your head
- Have the SENSE study device placed on your head to monitor bleeding for up to 48 hours
- Have your medical information collected

Study Details

Full Title
A Prospective, Two-Stage, Non-randomized, Multi-center Within Patient Comparison Study to Evaluate the SENSE Device?s Ability to Monitor Intracranial Hemorrhage
Principal Investigator
Emergency Medicine Specialist
Protocol Number
IRB: PRO00108101
NCT: NCT04642443
Phase
Phase N/A
ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate
Contact the Duke Recruitment Innovation Center
MyResearchPartners@duke.edu
or
919-681-5698