Tempus Pro Monitor Registry

Philips

Status: Completed

Conditions: Emergency Care; Sudden Cardiac Arrest

Treatments: Diagnostic Test: Standard of Care

Study type: Observational

Funder types: Industry; Other

Identifiers

NCT05587764

CCTCRDTTempusProRegi20211168

Details and patient eligibility

About

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

Full description

This observational study is to collect real-world data on the safety and performance of the Tempus Pro device, its accessories and the IntelliSpace Corsium telemedicine software device when used according to its intended purpose and the instructions for use, when used for patient monitoring.

Enrollment: 103 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients monitored by using Tempus Pro during pre-hospital care (ambulance transportation)

One or more 12-lead ECG recorded

Use of 3 or more of the following sensors to measure vital signs

• NIBP (Non-Invasive Blood Pressure)
• HR (Heart Rate)
• SpO2 (Oxygen Saturation)
• PVI (Pleth Variability Index)
• SpCO (Carboxyhemoglobin)
• SpOC (Oxygen Content)
• SpHb (Total Hemoglobin)
• SpMet (Methemoglobin Saturation)
• EtCO2 (End-tidal Carbon Dioxide)

Exclusion criteria

• None defined

Trial design

103 participants in 1 patient group

Standard of Care

Description:

Standard of Care for emergency care

Treatment:

Diagnostic Test: Standard of Care