Vital Sign Monitor Device Validation - WARD
Rigshospitalet, Denmark
1,000 participants
Oct 24, 2023
OBSERVATIONAL
Conditions
Summary
Aim: to assess the validity of CE/FDA approved vital sign monitor devices for clinical use in clinical setting. Patients: up to 1000 medical and/or surgical patients will be included Intervention: Studies with various wirless or novel vital sign monitor devices control: Golden standard measurements or clinical standard devices Outcome: Agreement assessed by bias and limits of agreement between Intervention and control device.
Eligibility
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Interventions
Devices that are to be introduced into the clinic but where data from clinical relevant conditions such as complications are lacking to assess the validity under clinical conditions
Locations(2)
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NCT06106516