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NCT Number: NCT07309809

Portrait Mobile Monitoring Solution V2.0 External Evaluation

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.

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Key information

Conditions

Monitoring

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

West Middlesex University Hospital

London, England, TW7 6AF, United Kingdom

About this study

Subjects will be enrolled from a general hospital ward to receive continuous monitoring for up to 72 hours by the Portrait Mobile Monitoring Solution V2.0. After the completion of that monitoring, both the clinician and the subject will complete a feedback survey about their experience with the device. The surveys along with raw data from the device will be collected from each subject.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Continuous Monitoring

Device

Subjects will have vital signs continuously monitored for up to 72 hours with the study device

Primary outcomes

  1. Collection of user feedback surveys from Clinicians

    Time frame: Up to 72 hours

    Number of clinician feedback surveys collected at the end of each shift for clinicians overseeing care of subjects receiving continuous vital signs monitoring.

  2. Collection of Subject Survey

    Time frame: up to 72 hours

    Number of subject surveys collected from study participants at the end of their continuous monitoring

Secondary outcomes

  1. Collection of raw parameter data from Portrait Mobile Device

    Time frame: up to 72 hours

    Collection of electronic waveforms and device logs from the investigational device for the entire monitoring period for each subject.

Study contacts

Contact information is provided by the study sponsor or research team.

Meghan Terry

CONTACT

[email protected]

262-290-6037

Sponsors and collaborators

Lead sponsor

GE Healthcare

Industry

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Dec 30, 2025
Registry last updated
Jun 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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