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NCT Number: NCT06453733

Crainio Non-invasive ICP Monitor for TBI

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.

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Key information

Age range

16 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Royal London Hospital

London, England, E1 1BB, United Kingdom

Location status: Recruiting

Location contact

Christopher Uff, Dr

PRINCIPAL_INVESTIGATOR

Christopher Uff, Prof

CONTACT

[email protected]

020 3594 2797

Maria Roldan, Dr

CONTACT

[email protected]

07737000015

Maria Roldan, MSc

SUB_INVESTIGATOR

About this study

Intracranial pressure (ICP) is routinely monitored in patients suffering from traumatic brain injury (TBI). Raised ICP can result in compression of the cerebral vasculature and subsequent reduction in oxygen and nutrient delivery to the brain leading to significant morbidity and mortality. In fact, raised ICP is the most common cause of death in patients with severe TBI.

Standard ICP monitoring requires insertion of a cranial bolt into the skull through which an electrical transducer is inserted. Alternatively, an intra-ventricular catheter is inserted through a burr hole. Both of these monitoring methods are associated with risks including haemorrhage and infection, as well as delay in establishing emergency monitoring and limiting it to hospitals that have neurosurgery.

There has been much research in recent years to find a method for measuring intracranial pressure noninvasively (nICP), including measurement of pressure in the retinal veins, measurement of eardrum displacement, transcranial Doppler ultrasonography and imaging-based solutions. These methods all require considerable user intervention and are non-continuous.

This project aims to collect cerebral photoplethysmogram signals and concurrent invasive ICP measurements from patients with traumatic brain injury to develop Crainio machine learning (ML) algorithms. The core intellectual property (IP) of this continuous external monitoring ICP system was originally developed by academics in the lab of Professor Kyriacou at City, University of London. Crainio is a spin-out company that was created to industrialise and commercialise this research on an exclusive basis.

The 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 estimate an absolute value of ICP.

The basic science behind this method for measuring ICP is that changes in the extramural arterial pressure affect the morphology of the recorded optical pulse, so analysis of the acquired signal using an appropriate algorithm will enable calculation of nICP. The reported nICP will provide screening at the triage stage, indicating the need for imaging or rapid intervention (such as haematoma evacuation) and guide head injury management, notably ICP-targeted treatment regimes. Ultimately this could lead to significant improvements in secondary injury-related mortality, length of hospital stay and reduced post-trauma disability.

This feasibility study aims to collect the clinical data with which to train the nICP algorithms to the point that they can detect raised intracranial pressure (ICP>20 mmHg) with sufficient sensitivity and specificity that Crainio device can be regulated for clinical use.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of traumatic brain injury.
  • Adults (aged between 16 and 99, male and female)
  • TBI patients admitted to the Royal London Hospital.
  • Patients having invasive ICP monitoring as part of their normal medical treatment.

Exclusion criteria

  • Forehead skin is not intact.
  • Decompressive craniectomy patients.
  • Open external ventricular drainage (EVD) treatment.
  • Patients who will unlikely survive the following twelve hours.

Treatment and study plan

Crainio

Device

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.

Other names: nICP probe, Crainio system

Primary outcomes

  1. Sensitivity

    Time frame: 12 hours record per patient

    Generate a nICP model offline with a sensitivity above 90% to discriminate ICP values over 20 mmHg.

  2. Specificity

    Time frame: 12 hours record per patient

    Generate a nICP model offline with a specificity above 90% to discriminateICP values over 20 mmHg.

Secondary outcomes

  1. Skin tone through Fitzpatrick scale

    Time frame: 1 classification per patient (3 minutes)

    Evaluating the effect on the nICP model of patient-related factors such as the skin tone.

  2. Skull thickness through CT scan

    Time frame: 1 measurement per patient (3 minutes)

    Evaluating the effect on the nICP model of patient-related factors such as the skull thickness.

  3. Skull density through Age stratification analysis

    Time frame: 1 classification per patient (1 minute)

    Evaluating the effect on the nICP model of patient-related factors such as the skull density.

  4. Device usability

    Time frame: 1 form per patient (5 minutes)

    Customised form to assess the acceptance of the device by the healthcare proffesionals.

  5. Advers effects and events

    Time frame: 12 hours record per patient

    Evaluate the device safety by monitoring the development of possible advers effects or events in the patients while data is acquired

Study contacts

Contact information is provided by the study sponsor or research team.

Jeremy Holland, Dr

CONTACT

[email protected]

0779 626 5994

Sponsors and collaborators

Lead sponsor

Crainio Ltda

Industry

Collaborators

  • Barts & The London NHS Trust
  • City, University of London
  • Innovate UK

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 12, 2024
Registry last updated
Mar 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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