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Wireless monitoring for recognition of patient deterioration - Checkpoint Cardio

Conditions
Monitoring patients with wireless wearable sensors
Registration Number
DRKS00024895
Lead Sponsor
niklinik RWTH Aachen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
25
Inclusion Criteria

Elective major abdominal surgery with planned postoperative intensive care stay for at least one night

Exclusion Criteria

-Known allergy/intolerance to adhesives in ECG electrodes,
-Implanted active medical devices (pacemakers or an implanted cardioverter defibrillator - ICD).
-Isolated patients (in case of MRE colonization or immunosuppression).

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison between each of the vital signs measured by the sensors (heart rate, respiratory rate, cuffless blood pressure measurement, and oxygen saturation) and the standard (wired) monitoring system used in the ICU.
Secondary Outcome Measures
NameTimeMethod
Occurrence of deterioration events requiring nurse intervention, and the deterioration score calculated by the system and hypothetical alarms generated by the test system depending on different thresholds for the score.<br>Usability evaluation of the system from the patient's perspective as a questionnaire.
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