Clinical Trials in the UK / NCT07309809
Starting soon
Not applicable
Portrait Mobile Monitoring Solution V2.0 External Evaluation
NCT07309809 · tracked via the Priya Life Science UK tracker
Condition(s) studied
Monitoring
Investigational drug(s) / intervention(s)
Continuous Monitoring
Continuous Monitoring: Subjects will have vital signs continuously monitored for up to 72 hours with the study device
Study summary
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
Inclusion Criteria:
1. Participant is age 18 years or older (≥18 years).
2. Participant must have the ability to understand and provide written informed consent.
3. Are being cared for in a hospital unit and are expected to remain in the unit for the duration of the study procedure.
4. Participant must be willing and able to comply with study procedures and duration.
Exclusion Criteria:
1. Known to be pregnant and/or breast feeding.
2. Diagnosed with infection requiring isolation.
3. Are immunocompromised.
4. Have previously participated in this study (no subject may participate more than once).
5. Subjects with Implantable Minute Ventilation Rate Responsive Pacemakers should be excluded from respiration rate monitoring.
Primary outcome measure(s)
- Collection of user feedback surveys from Clinicians — 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. - Collection of Subject Survey — up to 72 hours
Number of subject surveys collected from study participants at the end of their continuous monitoring
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| West Middlesex University Hospital | London | England |
More GE Healthcare trials in the UK
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07309809 on ClinicalTrials.gov ↗ ← All trials in the UK