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RECRUITING
NCT06453733
NA

Crainio Non-invasive ICP Monitor for TBI

Sponsor: Crainio Ltda

View on ClinicalTrials.gov

Summary

The clinical investigation aims to advance the Crainio device, designed for non-invasive intracranial pressure (ICP) monitoring. This feasibility study involves 54 participants over a 12-month period and seeks to collect cerebral photoplethysmogram signals alongside concurrent invasive ICP measurements in patients with traumatic brain injury. The primary objective is to establish the diagnostic accuracy of the Crainio device, aiming for at least 90% sensitivity and specificity in detecting raised ICP (above 20 mmHg). Secondary objectives include evaluating patient-related factors such as skin tone, skull thickness, and skull density, as well as the tolerability and acceptance of the device by both patients and healthcare professionals.

Official title: Crainio Non-invasive Intracranial Pressure Monitor for Traumatic Brain Injury: Product Development

Key Details

Gender

All

Age Range

16 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

54

Start Date

2025-05-15

Completion Date

2026-12-15

Last Updated

2026-03-18

Healthy Volunteers

No

Interventions

DEVICE

Crainio

Crainio device comprises a forehead-mounted sensor containing infrared light sources that can illuminate the deep brain tissue of the frontal lobe. Photodetectors in the sensor detect the backscattered light, which is modulated by pulsation of the cerebral arteries. A control unit processes the backscattered light (called the photoplethysmogram, PPG) and transmits it to a computer device to train ML models that will estimate ICP offline.

Locations (1)

Royal London Hospital

London, England, United Kingdom