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Pilot study to test a new radio-frequency and radar device for stroke detection

Assessment of Brain-injury using Radio-Frequency Induction and Microwave Spectroscopy

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN83538297
Enrollment
80
Registered
2023-04-19
Start date
2024-01-01
Completion date
Unknown
Last updated
2025-01-28

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

Conditions

Stroke Nervous System Diseases

Interventions

Current interventions as of 15/01/2025: We will conduct a pilot evaluation of a novel Magnetic Detection Electrical Impedance Spectroscopy (MDEIS) and Microwave Radar (MWR) device to determine its po

Sponsors

Northern Care Alliance NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Stage A: Healthy volunteers: 1. Aged 18 years or over 2. No significant health problems deemed by the investigator as likely to interfere with the study procedures or data analysis (e.g. previous or existing cerebral pathology) 3. Able to provide informed consent Stage B: Stroke patients: 1. Aged 18 years or over 2. Diagnosis of supratentorial ischaemic stroke or spontaneous intracerebral haemorrhage, within 72 h of symptom onset 3. Research MR scan can be performed within 5 days of admission 4. Likely to be able to safely complete study procedures, in the opinion of the lead clinical investigator or delegated clinical investigator

Exclusion criteria

Exclusion criteria: Stage A: Healthy volunteers: Any intracranial or extracranial metallic implant Stage B: Stroke patients: 1. Any intracranial metallic implant 2. Any extracranial metallic implant 3. Any contraindication to magnetic resonance scanning 4. Pre-existing intracranial pathology likely to interfere with measurements (e.g. previous stroke, tumour) 5. Any known condition which, in the opinion of the researcher, is likely to interfere with the planned recordings 6. Patient has undergone a neurosurgical procedure during the current admission, or this is planned within the next 24 h 7. Female patient who may be pregnant or is breastfeeding 8. Known allergy to electrodes 9. Any other significant disease or disorder which, in the opinion of the PI or his delegate, may put the participant at risk because of participation in the study, or may influence the result of the study, or the participant’s ability to participate in the study

Design outcomes

Primary

MeasureTime frame
Asymmetry index, determined from the microwave and MDEIS device, measured at a single timepoint in healthy volunteers and at 1 to 5 days after symptom onset in stroke patients

Secondary

MeasureTime frame
Transimpedance (Z), determined from the MDEIS device, measured at a single time point in healthy volunteers and at 1 to 5 days after symptom onset in stroke patients

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026