Detection of hEad Pulse for Ischemic StrOke Verification Study

NCT05602740 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2023-07-28

No results posted yet for this study

Summary

Prehospital providers encounter patients with suspected stroke frequently. Prehospital providers need tools to help triage large vessel stroke patients to comprehensive stroke centers. This device will identify large vessel stroke to ultimately improve triage decisions and optimize outcomes.

Conditions

  • Stroke, Acute

Interventions

DEVICE

Harmony

Passive recording of the head pulse

Sponsors & Collaborators

  • Wayne State University

    collaborator OTHER
  • MindRhythm, Inc.

    lead INDUSTRY

Principal Investigators

  • James Paxton, MD · Wayne State University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-15
Primary Completion
2023-10-01
Completion
2023-10-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05602740 on ClinicalTrials.gov