CompletedNCT06574867

REQUEST - RemotE Monitoring by viQtor Upon Implementation on a Surgical departmenT

Sponsor: Catharina Ziekenhuis Eindhoven

Trial Details

ConditionMonitoring, Post-operative Monitoring, Patient Safety, Healthcare Technology Implementation, Contiuous Vital Signs Monitoring
InterventionviQtor Wearable Monitoring Device
StatusCompleted
Participants500
Est. Completion31 July 2025
Last Updated1 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

Netherlands
View Registry Entry

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