Neuralert Stroke Monitor Trial

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
Neuralert Technologies LLC
Study ID
NCT07362303
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
22 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Neuralert Monitor — DEVICE
    The Neuralert monitoring system, a non-invasive device worn on each wrist, is designed to provide continuous monitoring for asymmetry in the extremities, sending an alert to healthcare workers upon identification, thus expediting recognition of stroke.

Study Details

The Neuralert monitoring system, a non-invasive device worn on each wrist, is designed to provide continuous monitoring and expedited recognition of stroke by identifying asymmetry in the extremities, facilitating patient treatment and improving outcomes. This study is designed to evaluate the safety and effectiveness of the Neuralert Monitor. This study aims to show that the device produces fewer than 2 false alarms per patient per day on average, and that the device detects stroke with a sensitivity significantly greater than a device producing 2 random alerts per day.

Key Dates

Start date
Mar 26, 2026
Status verified
Mar 2026
Primary completion
Jan 15, 2028
Completion
Jul 15, 2028

Study Design

Enrollment
1,200 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: Cardiac Surgery Patients
    Device: Neuralert Monitor Device to identify upper extremity asymmetry in patients who are high risk for stroke.

Primary Outcome Measure

Efficacy of Device [ Time Frame: through study completion, an average of 2 years ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Hospital of the University of PennsylvaniaPhiladelphiaPennsylvania19103
Stephanie Cummings
215-995-0238

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