Neuralert Stroke Monitor Trial
Part of paid clinical trials in Philadelphia, Pennsylvania.
- Sponsor
- Neuralert Technologies LLC
- Study ID
- NCT07362303
- Status
- Recruiting
Conditions
- Stroke
- Surgery
Eligibility Criteria
- Sex
- ALL
- Age
- 22 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Neuralert Monitor — DEVICEThe 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 PatientsDevice: 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
- Brett Cucchiara, MD(215) 662-6738
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Hospital of the University of Pennsylvania | Philadelphia | Pennsylvania | 19103 |
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