Actively Recruiting
Vital Sign Monitor Device Validation - WARD
Led by Rigshospitalet, Denmark · Updated on 2025-04-06
1000
Participants Needed
2
Research Sites
270 weeks
Total Duration
On this page
Sponsors
R
Rigshospitalet, Denmark
Lead Sponsor
B
Bispebjerg Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Vital Sign Monitor Device Validation - WARD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Medical and/or surgical patients
- Willingness to participate in vital sign monitoring up to 76 hours
You will not qualify if you...
- No specific exclusion criteria defined for this study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Eske Kvanner Aasvang
Copenhagen, Denmark, 2100
Actively Recruiting
2
Bispebjerg Hospital
Copenhagen, Denmark, 2400
Not Yet Recruiting
Research Team
E
Eske K Aasvang, DMSci
CONTACT
C
Christian S Meyhoff, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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