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Microwave Imaging in NeuroTrauma

Microwave Imaging in NeuroTrauma (MINT) - a Feasibility Study Investigating Whether Microwave-based Scanning Technology Can Detect an Intra-cranial Bleed in Adult Head Injury Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05960279
Acronym
MINT
Enrollment
500
Registered
2023-07-25
Start date
2021-07-20
Completion date
2025-01-31
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Craniocerebral Trauma

Keywords

Head injury, Traumatic brain injury

Brief summary

The study aims to investigate whether microwave-based technology can be used as a bedside decision-making aid to identify patients who may have a bleed in their head. The MD100 is a microwave-based head scanner, developed for the purpose of detecting strokes. In clinical trials, it was noticed that the device performed better when the patient suffered a stroke due to a bleed. It was believed that this device had wider applications in trauma care. The MD100 has demonstrated a very high level of accuracy in detecting bleeds in small clinical trials in the non-acute setting. The device is supported by software that determines the presence of a bleed. This study will be set in the emergency department of major trauma centres. Patients that have sustained a head injury will be considered for enrollment into the study. Following a head CT scan, patients will be scanned by the MD100. The trial will run in two phases. In phase one: the findings from the patient's head CT scan will be used to trial the device and teach the software what it is scanning. In phase two: The MD100 will be tested to see whether it can concur with the findings of the patient's CT scan, this will be used to determine the accuracy and reliability of the device.

Interventions

DEVICEMD100

The MD100 (Medfield Diagnostics, Gothenburg, Sweden) consists of 8 antennas and measurement electronics integrated into a single device; rechargeable ion batteries power the instrument. The radiation transmitted from the device equals approximately 1% of the radiation emitted from a mobile phone. The device is non-invasive and small enough that it can be moved around with ease. The system transmits microwaves with an output of 0.2 milliWatts (mW) for less than 90 seconds. The power absorbed by the body is 100mW/kg which is a factor of 200 less than what is established by the existing safety standard for microwaves. A mobile phone output, by comparison, can be up to 250mW. The patient's head is placed in the instrument during measurement while the patient is supine. The procedure takes, on average, 5 minutes to perform.

Sponsors

Air Ambulance Charity Kent, Surrey, Sussex
CollaboratorUNKNOWN
St George's University Hospitals NHS Foundation Trust
CollaboratorOTHER
Medfield Diagnostics AB
CollaboratorUNKNOWN
King's College Hospital NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 18 and over. * Blunt head trauma * The patient has had a CT head scan

Exclusion criteria

* Patients with head injuries penetrating the skull * Patients with radiologically confirmed cervical spine fracture * Patients with radiologically confirmed depressed skull fracture and/or dislocation * Patients with implanted metal in or around their skull (including titanium places and surgical staples) * Confirmed pregnancy * Per the investigator's judgement, any condition or symptoms preventing the patient from entering the trial.

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of the MD100One yearThe MD100's proportion of true positives of intracranial bleeds detected in the head injured patient.

Countries

United Kingdom

Contacts

Primary ContactJack Barrett, BSc
jack.barrett@secamb.nhs.uk07871632555

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026