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Comparison of Vital Sign Monitoring using Wearable Biosensor versus standard patient monitor

Comparative Evaluation of Continuous Vital Sign Monitoring in Intensive care unit: Standard ICU Monitor Versus UbiqVue 2A Wireless Patient Monitoring System with Wearable Biosensor - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074587
Enrollment
30
Registered
2024-10-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Control Intervention1: Philips MP70 - ICU patient Monitor: Adult patients meeting the inclusion criteria will be monitored simultaneously with both the standard ICU monitor (Philips MP70) and the Ubiq

Sponsors

LifeSignals India Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients (18 years or older) admitted to the ICU. 2. Patients having an invasive arterial monitor (radial or femoral) as per their clinical condition. 3.Male and female

Exclusion criteria

Exclusion criteria: 1. Participants with active implantable medical devices such as pacemakers or implanted defibrillators. 2. Participants exposed to magnetic resonance (MR) environment. 3. Participants allergic to adhesive, electrode gel or non-woven materials. 4. Women with pregnancy

Design outcomes

Primary

MeasureTime frame
To assess whether the UbiqVue 2A wireless patch system is able to reliably measure vital signs continuously in the clinical setting, and to determine how well it compares to recorded measurements in standard ICU monitor.Timepoint: Continuous data will be recorded from both devices for up to 48 hours

Secondary

MeasureTime frame
aims to compare the accuracy and reliability of continuous vital sign monitoring using a standard ICU monitor with the UbiqVue 2A Wireless Patient Monitoring System over a 48-hour period.Timepoint: Continuous data will be recorded from both devices for up to 48 hours

Countries

India

Contacts

Public ContactDr Mathangi Krishnakumar

St Johnâ??s Medical College Hospital

mathangidoc@outlook.com9764062212

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026