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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05587764
Study type Observational [Patient Registry]
Source Philips Clinical & Medical Affairs Global
Contact
Status Enrolling by invitation
Phase
Start date April 25, 2024
Completion date June 28, 2024

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