REQUEST - RemotE Monitoring by viQtor Upon Implementation on a Surgical departmenT
Sponsor: Catharina Ziekenhuis Eindhoven
Trial Details
| Condition | Monitoring, Post-operative Monitoring, Patient Safety, Healthcare Technology Implementation, Contiuous Vital Signs Monitoring |
| Intervention | viQtor Wearable Monitoring Device |
| Status | Completed |
| Participants | 500 |
| Est. Completion | 31 July 2025 |
| Last Updated | 1 May 2026 |
Primary Outcome
Usability of the viQtor Monitoring Solution
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Adult patients (18 years and older). * Patients admitted to the surgical ward at Catharina Hospital Eindhoven. * Fluent in Dutch or English. * Willingness to participate in the study and to wear the viQtor monitoring device during their hospital stay. Exclusion Criteria: Patients with cognitive impairments. * Patients with allergies to metal or plastics. * Patients with significant deformities, swelling, irritation, degenerative changes, or edema of the upper arm. * Patients with implanted cardiac pacemakers, internal cardioverter defibrillators, or chronic resynchronization therapy devices. * Patients at risk of vascular compromise of the arm on which the device will be placed. * Patients with conditions that contraindicate the use of a blood pressure cuff or similar devices.
Trial Sites
Countries
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