New hospital monitor gets a test run
NCT ID NCT07309809
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new mobile device that tracks patients' vital signs continuously in the hospital. About 50 adult patients will use the device, and researchers will collect feedback from both patients and clinicians. The goal is to see how well the device works and gather data to improve future versions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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West Middlesex University Hospital
London, England, TW7 6AF, United Kingdom
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