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Tempus Pro Monitor Registry

NCT05587764 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 103

Last updated 2025-03-10

No results posted yet for this study

Summary

A multicenter, prospective and retrospective, observational, post market study.

Conditions

  • Sudden Cardiac Arrest
  • Emergency Care

Interventions

DIAGNOSTIC_TEST

Standard of Care

Standard of care for emergency events per local guidelines.

Sponsors & Collaborators

  • North American Science Associates, LLC

    collaborator UNKNOWN

  • Philips Clinical & Medical Affairs Global

    lead INDUSTRY

Principal Investigators

  • Richard Lyon, MB CHB (HONS) MD MRCP FRCEM · CONSULTANT IN EMERGENCY MEDICINE, NHS LOTHIAN

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-25
Primary Completion
2024-08-12
Completion
2024-08-12
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 NCT05587764 on ClinicalTrials.gov