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

Study acronym: OXYVIVO
StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary and study completion pushed from Dec 2026 to Jan 2027
    • Start date: Jun 2026 to Jul 2026
    v9
  2. Primary completion pushed from Jun 2026 to Dec 2026
    • Study completion moved earlier from Jan 2027 to Dec 2026
    • Start date: May 2026 to Jun 2026
    v8
  3. 2 versions Re-verified since Mar 17, 2026, no change to tracked fieldsv6-v7
  4. Start date: Jan 2026 to May 2026
    • Primary completion date: Feb 2026 to Jun 2026
    • Study completion date: Sep 2026 to Jan 2027
    • Study title shortened, about 10 words
    v5
  5. Start date: Aug 2025 to Jan 2026
    • Primary completion date: Sep 2025 to Feb 2026
    • Study completion date: Apr 2026 to Sep 2026
    v4
Show 2 earlier versionsHide 2 earlier versions
  1. Trial status: Recruiting to Not Yet Recruitingv3 Show 4 more changesShow less
    • Primary completion date: Aug 2025 to Sep 2025
    • Study completion date: Mar 2026 to Apr 2026
    • Start date: Jul 2025 to Aug 2025
    • Site details revised
  2. Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Jul 2025 to Aug 2025
    • Study completion date: Feb 2026 to Mar 2026
    • Start date: Jun 2025 to Jul 2025
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07037784
Lead Sponsor Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Conditions
(from sponsor)		 Physiological Parameters
Enrollment 102 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov