Biomarkers, Brain Injuries, Traumatic, Microwave Imaging
Conditions
Keywords
Microwave Imaging
Brief summary
This study will evaluate if traumatic intracranial hemorrhage can be safely ruled out by using a microwave scanner (MD100) in conjunction with a combination of different brain biomarkers analyzed in serum.
Detailed description
This is a prospective, open, multicentre trial that will enrol patients presenting to the Emergency Department (ED) because of isolated head trauma or head trauma as part of a multi trauma. Microwave scanning characteristics and biomarkers in patients with traumatic intracranial haemorrhage (TICH) (Group A) will be compared to patients with head trauma that do not have TICH (Group B). All adult patients with trauma to the head will be eligible for inclusion if a medical professional has evaluated the risk of spine injury. After additional physical examination, control of inclusion- and exclusion criteria and after informed consent has been acquired, the microwave measurement and blood sampling will be performed. Before enrolment in the study, and in the acute phase, one of the investigators or a member of the investigator staff must explain verbally the implications of study participation to the patient, and the patient is asked to give a verbal consent. As soon as is practically possible after the acute phase of the disease, the patient will sign and personally date the informed consent form. In cases where the patient is not capable to read and/or sign the informed consent, due to disability, an independent witness shall be present throughout the process of reading the written informed consent and any other information aloud and explained to the prospective patient. As an independent witness, healthcare professionals who are not responsible or in any way involved in the patient's care or treatment are accepted. The independent witness can sign on the behalf of the patient in the presence of the patient and the Investigator. More details of the informed consent procedure are described in this Clinical Investigation Plan, section 6.3. The microwave measurement will take less than five minutes (the duration of the actual measurement is about 1,5 min and will not interfere with the patient's standard of care). The Research Nurse or the Investigator documents all patient clinical trial information in the eCRF. Safety and usability will be evaluated throughout the trial, and a safety follow-up will be performed by the Research Nurse or Investigator approximately 24 hours after the measurement procedure. During the data processing phase of study, the result of the microwave measurement will be compared to the result of the biomarkers, CT examination and the patient's final diagnosis. As a control group, approximately 50 demographically matched healthy volunteers (Group C) will be asked to participate in the trial. The trial will provide knowledge of the predictive value of microwave measurement and biomarkers for the diagnosis of intracranial haemorrhages in the acute TBI phase.
Interventions
DEVICEMicrowave scanning of the head
A scan of the head will be performed with a microwave device to ascertain the likelihood of intracranial hemorrhage.
Sponsors
Medfield Diagnostics
Region Skane
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Caregiver)
Masking description
No results of the biomarker assays or microwave scans will be visible to the care givers or the participants.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
(groups A and B): * Verbal Informed Consent in the acute phase. * Signed Informed Consent Form after the acute phase. On behalf of the patient, independent witness signed informed consent (in cases where the patient is unable to sign). * Acute trauma patient with suspected head injury * Time from injury to measurement procedure not longer than 8 hours 15 min * Head CT prescribed by treating physician * Patient is ≥ 18 years of age * Patient is deemed clinically stable
Exclusion criteria
(groups A and B): * Patient has suspected cervical spine fracture, per the Investigator's judgement * Patient has by CT confirmed cervical spine fracture * Patient has confirmed skull fracture with risk for dislocation. * Patient has a shunt or other foreign object implanted intracranially (if known by medical records) * Patient has agraffes or other metal parts, thick bandage (\>1cm), or other foreign materials attached to the head that are deemed to interfere with the diagnostic procedure. * Patient diagnosed with a condition associated with risk of poor protocol compliance * The measurement procedure is deemed to interfere with the standard of care * Other condition or symptoms preventing the patient from entering the trial, per the investigator´s judgment Inclusion Criteria (Group C): * Patient is ≥ 18 years of age * Signed informed consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Ability to detect intracranial hemorrhage | 3.5 years | The ability of the device MD100, with and without brain biomarkers (Aβ40, Aβ42, GFAP, H-FABP, S100B, NF-L, NSE, UCH-L1 and IL-10) to detect traumatic intracranial haemorrhage, as measured by the area under the receiver operating characteristics curve. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Estimating anatomic position of intracranial hemorrhage | 3.5 years | The accuracy for estimating the position of intracranial hemorrhage with microwave data. |
| Estimating volume of intracranial hemorrhage | 3.5 years | The accuracy for estimating the volume of intracranial hemorrhage with microwave data. |
| Adverse events of microwave scan | 3.5 years | Any adverse events occurring within 24 hours of microwave scan |
Countries
Sweden
Contacts
Primary ContactTomas J Vedin, MD, PhD
Backup ContactJacob Lundager Foberg, MD, PhD
Outcome results
None listed