Monitoring of Patient Physiological Parameters in Real Life Using OXYFLEX® Biosensors Versus Standard Monitoring

Starting soon · Not applicable

Conditions studied: Physiological Parameters

In brief

The purpose of this study is to use the OXYFLEX® device in real care conditions during the hospital management of a population of patients from various hospital services. These services include patients from the severe trauma pathway, intensive care, the polyvalent intensive care unit, and the operating room. The objective is to assess the reliability of the data collected by the OXYFLEX® biosensor compared to those obtained from standard monitoring used in these different services and conditions.

Key facts

Study ID

NCT07037784

Run by

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

People needed

102

Starts

2026-07-01

Expected to finish

2027-01-01

Last updated by the study team

2026-07-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patient (≥ 18 years old);
• Patient taken care of :
• in severe traum pathway in the emergency services department
• or in the operating room for a general anesthesia procedur or locoregional anesthesia planned for a surgical duration grater than 2 hours
• or admitted to intesive care/ general intensive care units.

You may not qualify if…

• Opposition from the patient or their family to participate in the research ;
• Pregnant, parturient or breastfeeding woman ;
• Patient under judical protection (guardianship, curatorship …) or legal safeguarding ;
• Inability to wear the headband and the sensor (in particular : intracranial neurosurgery, othorhinolaryngology or maxillofacial surgery, debilitating trauma to the head or face …) ;
• Any other reason that, in the investigator's opinion, could interfere with the evaluation of the study objectives.

Where it is running

• HIA Ste Anne — Toulon, Var, France

Full record on ClinicalTrials.gov

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