Portrait Mobile Monitoring Solution V2.0 External Evaluation
ConditionMonitoring
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGE Healthcare
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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).
Trial design
Treatments tested in this trial
- Continuous Monitoring
Treatment groups
50 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov