The Neuralert Stroke Monitor Pilot Trial
Sponsored by Neuralert Technologies LLC
About this study
This trial aims to demonstrate that the Neuralert Monitoring System will detect strokes before they would be identified by current standard of care. Each patient will be monitored for up to five days, depending on device connectivity or battery duration. Each monitoring session will consist of wearing a Neuralert device on each arm. For this pilot trial, we are interested in learning about Wi-Fi connectivity, successful data transmission, integration into clinical workflow, usability and tolerability.
Where this study is enrolling
- I'm interested
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania
Who can participate
Exclusion criteria
- ✕(all must be no)
- ✕1. Any medical or psychological conditions that, in the opinion of the investigator, would compromise the subject's safety or successful participation in the study
- ✕2. Baseline preoperative asymmetric upper extremity weakness as assessed by the Investigator, defined as a differential in the NIHSS upper extremity motor score between the two arms of \>0
- ✕3. Above the wrist amputation
- ✕4. Unwilling to provide informed consent or no legally authorized representative willing to provide consent if the patient is unable
- ✕5. Currently imprisoned
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.