Actively Recruiting
Handheld Point of Care Electro-Diagnostic Device
Led by Indiana University · Updated on 2026-02-09
30
Participants Needed
1
Research Sites
46 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There are currently several products offering POC EEG, intended to be deployed on each patient individually and continuously. The investigators propose studying a different approach by using a migrating POC electrodiagnostic device that is deployed directly by the onsite provider and is actively used, like other POC devices, to acquire real-time diagnostic insight and facilitate immediate medical decision making. This can significantly shorten time to treatment which in several neurological and neurosurgical conditions, and thus, can significantly improve patient outcome. The investigational POC investigational device is based on a handheld limited electrode array, complemented by various stimulation modalities such as SSEP, VEP and BAEP, and potentially other sensors. For this study, the investigators intend to use readily available industry standard stimulators and only use the proposed POC investigational device to acquire and analyze the data. The POC investigational electrodiagnostic prototype was assembled using OpenBCI8 electronic board and electrodes, based on ADS 129X chip by Texas Instruments, that was shown to provide an adequate low-cost solution for electrodiagnostic data acquisition.
CONDITIONS
Official Title
Handheld Point of Care Electro-Diagnostic Device
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years old or above
- Seen inpatient or in outpatient service at IU Health facilities - Methodist Hospital, and the Neuroscience Center, by a Neurology and/or Neurosurgery consultant as part of their SOC
- The participant has capacity to sign consent or has an assigned LAR (Legally Authorized Representative - Spouse, parent, sibling, etc.) able to consent on their behalf
You will not qualify if you...
- Pregnant woman
- PI unblinded by participant or LAR regarding indication or clinical data
- Burns or extensive skin lesions
- Implanted stimulation devices (any)
- Participant without standard imaging and, or other paraclinical SOC investigations to be comparable to the POC investigational device acquired data
- Significant acute or chronic medical, neurologic, or other illness in the patient that, in the judgment of the PI, could compromise subject safety, limit the ability to complete the study, and/or compromise the objectives of the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Indiana University Health
Indianapolis, Indiana, United States, 46202
Actively Recruiting
Research Team
S
Sergiu Abramovici, MD
CONTACT
L
Lauren Perrey-Moore, BSN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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