Evaluation of the viQtor Monitoring Solution on Surgical Wards (NCT06574867) | Clinical Trial Compass
CompletedNot Applicable
Evaluation of the viQtor Monitoring Solution on Surgical Wards
Netherlands500 participantsStarted 2024-10-01
Plain-language summary
The REQUEST study aims to evaluate the use of a new wireless monitoring device, called the viQtor solution, on a surgical ward in Catharina Hospital Eindhoven. This device continuously tracks vital signs, such as heart rate, breathing rate, and blood oxygen levels, in patients after surgery. The goal is to see if the viQtor solution can help detect health problems earlier and reduce the workload for nurses by minimizing the need for manual checks. The study will involve 500 patients and will take place over 7 months.
Who can participate
Age range18 Years
SexALL
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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.