Corsano CardioWatch 287-2 for Improved E-health MOnitoring Evaluation Study.

Corsano CardioWatch 287-2 for Improved E-health MOnitoring Evaluation Study. - EMOC study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON57542

Enrollment

Registered

2025-05-19

Start date

2026-04-10

Completion date

Unknown

Last updated

2026-06-08

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

Conditions

Cardiac surgery Open heart surgery

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: >= 18 years old; able to provide consent. following the peri-operative E-health care pathway receiving open heart surgery

Exclusion criteria

Exclusion criteria: Unable to wear the Corsano CardioWatch 287 due to reasons such as allergic reactions, wounds, amputations etc.; Unable to receive blood pressure measurements per cuff due to lymphedema, amputation, dialysis shunt, wounds, etc.; Pregnant women; Breastfeeding women; Unable or not willing to sign informed consent; Significant mental or cognitive impairment.

Design outcomes

Primary

Measure	Time frame
Primary outcomes 1. Mean difference and its SD (Standard Deviation) of the parameters measured including MEWS (Modified Early Warning Score) by the Corsano CardioWatch 287-2 and 'The Box'.	—

Secondary

Measure	Time frame
Secondary outcomes: 1. Mean difference and its SD of the Device User-Friendliness Comparison Survey between the Corsano CardioWatch 287-2 compared to 'The Box' in the E-health care pathway 2. Mean difference and its SD Usability of the Usability Assessment Survey between the Corsano CardioWatch 287-2 compared to 'The Box' in the E-health care pathway	—

Countries

Netherlands

Outcome results