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Detection of Area of Ischemia in Patients With Subacute Stroke Via a Hybrid EEG-fNIRS Brain-computer Interface

Detection of Area of Ischemia in Patients With Subacute Stroke Via a Hybrid EEG-fNIRS Brain-computer Interface

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03034902
Enrollment
5
Registered
2017-01-27
Start date
2017-02-09
Completion date
2017-06-20
Last updated
2022-04-27

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

Conditions

Stroke

Brief summary

The purpose of this research study is to determine whether a combined electroencephalography (EEG) and functional near infrared spectroscopy (fNIRS) recording is able to detect changes in brain activity and blood flow after stroke.

Interventions

DEVICECombined EEG and fNIRS

The EEG+NIRS recordings will be obtained via an extended EEG cap that is applied to the subject's head. Changes in neuronal activity and hemodynamics will be measured. The EEG component is the microEEG by BioSignal Group, UA. The fNIRS component is the NIRScout 24x32, NIRx Medizintechnik GmbH, Germany

Sponsors

University of Houston
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Eligibility

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

Inclusion criteria

* All patients with a subacute ischemic stroke with symptom onset within 8 weeks * Must have a measurable deficit on the National Institute of Health Stroke Scale (NIHSS) * Able to give and sign informed consent

Exclusion criteria

* Aphasia * Underlying dementia * Any chronic neurological disorder * Malignancy * Non-ambulatory (ambulation with assistance will be included) * Modified Rankin Score (mRS) \> 3

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with abnormal blood flow as assessed by fNIRSimmediately at the time of combined EEG and fNIRS for up to 60 minutesAbnormal blood flow is determined by comparing a part of the patient's brain not affected by stroke to a part of the patient's brain affected by stroke.
Number of participants with abnormal neuronal activity as assessed by EEGimmediately at the time of combined EEG and fNIRS for up to 60 minutesAbnormal neuronal activity is determined by comparing a part of the patient's brain not affected by stroke to a part of the patient's brain affected by stroke.

Countries

United States

Outcome results

None listed

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