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Clinical Trials/NL-OMON54951
NL-OMON54951
Completed
Not Applicable

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

Divisie Vitale Functies0 sites25 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Divisie Vitale Functies
Enrollment
25
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Divisie Vitale Functies

Eligibility Criteria

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
  • \* a need for contact isolation (to avoid any risk of cross\-contamination)

Outcomes

Primary Outcomes

Not specified

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