Portrait Mobile Monitoring Solution V2.0 External Evaluation

Starting soon · Not applicable

Conditions studied: Monitoring

In brief

The purpose of this study is to collect and assess feedback from the users regarding the functionality and performance of the Portrait Mobile Monitoring Solution V2.0. In addition, this study aims to collect raw parameter data from the investigational devices for use in current and future Portrait Mobile development, including engineering purposes as deemed appropriate by the Sponsor.

Key facts

Study ID

NCT07309809

Run by

GE Healthcare

People needed

50

Starts

2026-07-01

Expected to finish

2026-10-01

Last updated by the study team

2026-06-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant is age 18 years or older (≥18 years).
• Participant must have the ability to understand and provide written informed consent.
• Are being cared for in a hospital unit and are expected to remain in the unit for the duration of the study procedure.
• Participant must be willing and able to comply with study procedures and duration.

You may not qualify if…

• Known to be pregnant and/or breast feeding.
• Diagnosed with infection requiring isolation.
• Are immunocompromised.
• Have previously participated in this study (no subject may participate more than once).
• Subjects with Implantable Minute Ventilation Rate Responsive Pacemakers should be excluded from respiration rate monitoring.

Where it is running

• West Middlesex University Hospital — London, England, United Kingdom

Full record on ClinicalTrials.gov

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