Validation of vital sign monitor devices in clinical settings
Vital Sign Monitor Device Validation - WARD
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 |
|---|---|
| Enrollment | 1000 (estimated) |
| Sex | All |
| Sponsor | Rigshospitalet, Denmark Academic / other |
| Locations | 2 sites (Copenhagen and 1 other locations) |
| Trial ID | NCT06106516 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study include medical and surgical patients undergoing procedures requiring vital sign monitoring.
Not a fit: Patients who do not require vital sign monitoring or are not undergoing surgery may not benefit from this study.
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 performed: Other studies have shown success in validating novel monitoring devices, indicating that this approach has potential based on previous findings.
Eligibility criteria
Show full inclusion / exclusion criteria
No inclusion or exclusion criteria
Where this trial is running
Copenhagen and 1 other locations
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.