Technology, design, and data are valuable metrics, but it’s clinical outcomes that move the needle.
See what our clinical evidence says about the use of Sense technology for field assessment and hospital monitoring.
360 data points collected
Entire cranial vault analyzed
Bleed detection from 1ml up to 60ml
Range of Bleeds
First in Human Trial Successfully Completed
SENSE Neuro Diagnostics Inc. has successfully completed its ‘first in human’ trial of the SENSE device in intracranial hemorrhage (ICH) patients in the neurological intensive care unit. The objective of this small pilot trial was the safety and usability of the device in the clinical setting.
An additional objective was the detection of > 3 ml of ICH expansion (HE) using a non-invasive RF-based technique. There were no significant adverse events (SAEs) from the use of the device during continuous patient monitoring for up to 72 hours. Although the trial was small (n=10), the concordance of the SENSE readings with CT was 100% for the presence or absence of HE.
We look forward to the initiation of our pivotal clinical trial of the device in August of this year, as the COVID 19 pandemic permits.
9 patients, Compared SENSE to CT Scans at baseline, 12 and 72 hours
No false positives, No false negatives
We are driven by our mission and are committed to impacting people’s lives and enhancing neurological health globally. You can be part of our journey too.