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Vital Sign Monitor Device Validation - WARD
Sponsor: Rigshospitalet, Denmark
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.
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
1000
Start Date
2023-10-24
Completion Date
2028-12-31
Last Updated
2025-04-06
Healthy Volunteers
Yes
Interventions
novel vital sign monitor
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)
Eske Kvanner Aasvang
Copenhagen, Denmark
Bispebjerg Hospital
Copenhagen, Denmark