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Wireless monitoring for recognition of patient deterioration - Checkpoint Cardio

Wireless monitoring for recognition of patient deterioration - Checkpoint Cardio - NIGHTINGALE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00024895
Enrollment
25
Registered
2021-04-28
Start date
2021-04-21
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Monitoring patients with wireless wearable sensors

Interventions

Group 1: Wireless monitoring of vital signs for five days after surgery

Sponsors

Uniklinik RWTH Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

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).

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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. Usability evaluation of the system from the patient's perspective as a questionnaire.

Countries

Germany

Contacts

Public ContactLisa Hartung

Uniklinik RWTH Aachen

lhartung@ukaachen.de0241 8089357

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026