Clinical Evaluation of the Vital Signs Monitoring System (VSMS)

Status Recruiting

Clinical Trial Summary

This is an observational, cohort-based, single-site, prospective study conducted in accordance with ISO 14155-1:2003 and ISO 14155-1:2011. The primary objectives are to evaluate the accuracy of the device's measurements/readings in comparison to a gold standard or standard of care patient monitor.

Clinical Trial Description

This is an observational, cohort-based, single-site, prospective clinical study enrolling up to 100 patients who are hospitalized in the internal ward. There is no control group.

The primary objectives of the study are:

1. Evaluate the body temperature measured by the ear unit and validate its accuracy.

2. Evaluate the accuracy of SPO2 signals and results by comparing the readings to a gold standard device with a finger sensor.

3. Evaluate the ECG and respiration signals recorded by the patch device by comparing them to the signals recorded by a patient monitor with standard leads.

The secondary objectives of the study are:

4. Usability - evaluate the ease of use of the device by medical staff and patients (e.g., positioning, activation, replacement of patch, understanding processes and requirements).

5. Evaluate the signals quality and the patch adherence after 5 - 7 days on the chest.

The study will assess the safety and effectiveness of the Vital Signs Monitoring System (VSMS) for its intended use/proposed indications. Data will be collected while the VSMS is adhered to each patient for the entire hospitalization period, up to 7 days. There is no follow-up required. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03206528
Study type	Observational
Source	G Medical Innovations Ltd.
Contact	Anat Alon
Phone	972 8-977-9999
Email	alona@asaf.health.gov.il
Status	Recruiting
Phase	N/A
Start date	April 25, 2017
Completion date	July 31, 2017

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