The goal of this prospective, comparative, multi-centre interventional clinical investigation, is to evaluate the performance of the Thermodiag® medical device, compared with reference methods, for continuous measurement of core temperature in critical care patients. The main question it aims to answer is to develop non-invasive alternatives to the current methods of measuring core body, to reduce health risks, and overcome various other limitations (as infection, bleeding, thrombosis and local reactions).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
60
In intensive care Medics will use a reference medical device and Thermodiag®. Simultaneous and synchronised measurements will be taken every minute.
Centre Hospitalier De Fleyriat
Bourg-en-Bresse, France
Centre Hospitalier Intercommunal - Nord-Ardennes
Charleville-Mézières, France
Hôpital Privé de l'Ouest Parisien
Trappes, France
Hôpital Nord Franche-Comté
Trévenans, France
Body temperature Measurement
The degree of agreement between the two medical devices (Thermodiag® versus reference method in the hospital unit) will be assessed (expected measure is less than 0.1°C).
Time frame: Every minute from the enrollment to the end of medical treatment (estimated time : 8 days)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.