Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
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
| Measure | Time 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
| Measure | Time 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
St Johnâ??s Medical College Hospital