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Usability Study of CEREBO® - A Novel Non-invasive Intracranial Bleed Detector

Traumatic Brain Injury Clinical Trial

Official title:
Summative Usability Study of CEREBO® in Traumatic Brain Injury Patients to Determine Ease of Use, Ease of Learning and Satisfaction

Clinical Trial Summary

Traumatic Brain Injury (TBI) is the leading cause of death and disability across the globe. Time from injury to treatment is the most critical factor that determines the patient's recovery. Mild TBI with no apparent symptoms are often left undiagnosed, thus delaying the treatment and hence recovery. CEREBO® is a non-invasive, rapid, near-infrared based, point-of-care device that can detect an intracranial bleed at an early stage.

Clinical Trial Description

This prospective study determines the usability of CEREBO® to detect the intracranial hematoma. The operators will receive a training session before the study and will be evaluated at the end of the study through a survey questionnaire for ease of use, ease of learning and satisfaction. Each operator will examine at least 10 subjects with CEREBO®. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05340114
Study type Interventional
Source Bioscan Research Pvt. Ltd.
Contact Bioscan Research
Phone 7948994429
Email info@bioscanresearch.com
Status Not yet recruiting
Phase N/A
Start date April 25, 2022
Completion date May 31, 2023
View Details
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