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COMPLETED

NCT05587764

Tempus Pro Monitor Registry

Sponsor: Heartstream US LLC

View on ClinicalTrials.gov

Summary

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

Official title: A Post Market Clinical Follow-up Study to Evaluate the Safety and Clinical Performance of the Tempus Pro, a Multi-parameter Vital Signs Monitoring Device With Specific Reference to ECG Recordings and Data Transmission Using Telemedicine

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

103

Start Date

2024-04-25

Completion Date

2024-08-12

Last Updated

2026-08-21

Healthy Volunteers

Conditions

Sudden Cardiac Arrest Emergency Care

Interventions

DIAGNOSTIC_TEST

Standard of Care

Standard of care for emergency events per local guidelines.

Locations (1)

Philips

Pittsburgh, Pennsylvania, United States