Early recognition of deterioration in high-risk patients using continuous remote wireless monitoring: a clinical observation study with the Checkpoint Cardio system

Completed

• Conditions: Dit betreft een observationele studie met continue metingen van vitale functies bij patiënten met risico op adverse events, welke niet gerelateerd is aan een enkele aandoening of orgaansysteem; Not applicable

• Registration Number: NL-OMON54951
• Lead Sponsor: Divisie Vitale Functies

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 25

Inclusion Criteria

* All adult patients (>18 yr of age) who are at high risk for development of
serious adverse events receiving care at a surgical or acute medical ward.
* Minimum expected duration of hospital stay > 48h

Exclusion Criteria

* known allergy/skin irritation to the adhesives used in the recommended
commercially ECG electrodes (alternative electrodes may be offered).
* implanted active medical devices, such as a cardioverter defibrillator or a
pacemaker (to avoid potential interference between the different sensing
systems)
* a need for contact isolation (to avoid any risk of cross-contamination)

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified