CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 500 enrolled
Drug / intervention
viQtor Wearable Monitoring Devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06574867
NCT06574867N/ACompleted

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

Catharina Ziekenhuis Eindhoven·observational·Posted Aug 28, 2024·Updated May 1, 2026

In Brief

An observational study evaluating viQtor Wearable Monitoring Device for Monitoring and 4 related conditions. Completed, enrolled 500 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesNetherlands
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedAug 28, 2024
Enrollment StartOct 1, 2024
Primary CompletionJul 31, 2025
Study CompletionDec 1, 2025
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 1.8 years ago

Interventions

viQtor Wearable Monitoring Devicedevice

The viQtor device is a wearable medical device designed for continuous monitoring of vital signs, including heart rate (PR), respiratory rate (RR), and blood oxygen saturation (SpO2). It is worn on the upper arm and transmits data wirelessly to a cloud-based platform. This device is being evaluated as part of the standard monitoring protocol for post-operative patients in a surgical ward setting.