Validation of vital sign monitor devices in clinical settings
Official title: Vital Sign Monitor Device Validation - WARD
Run by Copenhagen University Hospital, Rigshospitalet · NCT06106516 · Data updated 2026-11-12
This study is testing new vital sign monitor devices to see if they work as well as the standard equipment used in hospitals for patients undergoing surgery.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Copenhagen University Hospital, Rigshospitalet Academic / other |
| Locations | 2 sites (Copenhagen and 1 other locations) |
| Status | Recruiting |
| Started | October 24, 2023 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | April 6, 2025 |
| Trial ID | NCT06106516 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study include medical and surgical patients undergoing procedures requiring vital sign monitoring.
✕Probably not a fit
Patients who do not require vital sign monitoring or are not undergoing surgery may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to assess the validity of CE/FDA approved vital sign monitor devices for use in clinical settings. Up to 1000 medical and surgical patients will participate, with various wireless or novel devices being tested against standard measurements. The agreement between the new devices and established clinical standards will be evaluated through bias and limits of agreement. The study will take place over a period of up to 76 hours, collecting vital sign data before, during, and after surgical procedures.
Why it matters
Potential benefit: If successful, this study could enhance the reliability of vital sign monitoring in clinical settings, leading to improved patient outcomes.
How similar studies have gone: Other studies have shown success in validating novel monitoring devices, indicating that this approach has potential based on previous findings.
Who can join: the full rules
Show full inclusion / exclusion criteria
No inclusion or exclusion criteria
Where it's running
-
Eske Kvanner Aasvang
Copenhagen, Denmark Recruiting -
Bispebjerg Hospital
Copenhagen, Denmark Not yet recruiting
Study contacts
- Study coordinator: Eske K Aasvang, DMSci
- Email: eske.kvanner.aasvang.01@regionh.dk
- Phone: +4526232076
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.