Actively Recruiting

Age: 18Years +
All Genders
NCT07293299

The PneumoRator Study

Led by University Hospital Southampton NHS Foundation Trust · Updated on 2025-12-19

50

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University Hospital Southampton NHS Foundation Trust

Lead Sponsor

U

University of Southampton

Collaborating Sponsor

AI-Summary

What this Trial Is About

Healthcare workers measure heart rate, blood pressure, temperature, oxygen levels and breathing rate to monitor how unwell a patient is. All these apart from breathing rate are now normally measured by machines. But there still isn't a machine that does this well enough for breathing rate to be used in most places. The machines that do exist are either uncomfortable or don't work well on patients who are moving. Instead, a healthcare worker will count the number of breaths a patient takes. This needs staff time and isn't very accurate. It is known that changes in breathing rate can happen any time. But healthcare systems normally only measure it every few hours because it takes time. Breathing rate could be monitored all the time, we might pick up people getting sick earlier and be able to treat them more quickly, which could save lives. A team at the University of Southampton has made a small device, called a PneumoRator, that gets stuck to onto a person's chest. Once stuck there it can measure their breathing rate and store or send that information wirelessly. The device has been tested on healthy volunteers but has never been tested on patients in hospital. In this study the team will put the device on patients having major operations. The investigators will record information already collected about patients during normal care. This includes their breathing rate using the best measurement we have, where a patient's breathing is measured by a gas they breathe out. The gas is carbon dioxide, and the measurement is called capnography. This way of measuring is only used in operating theatres and intensive care units but is a good way to check if the PneumoRator is accurate. The investigators want to attach the PneumoRator to patient's chests before they go to sleep for their operation and leave it there for the first few days after their operation. This will let them see how the PneumoRator compares to capnography and manual breath counting. It will also let them see how the device works at different times in the patient's journey. The investigators will look at the time when patients are asleep, when breathing is controlled by a machine. Then when patients wake up investigators can measure with both capnography and the PneumoRator. Finally, when patients go to the high dependency ward, investigators will compare it against manual counting. The study team will also ask patients how they found wearing the device and any problems they found. With this information the investigators hope to show the PenumoRator is accurate at measuring breathing rate and comfortable for patients. This will help them get the device approved for use in hospitals and other places where breathing rate needs to be measured accurately.

CONDITIONS

Official Title

The PneumoRator Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have undergone or are referred for CPET
  • Scheduled for elective surgery with expected postoperative hospital stay longer than 24 hours
  • Planned admission to the Surgical High Dependancy Unit (SHDU)
  • Will receive invasive arterial pressure monitoring as part of routine care
  • Aged 18 years or older
  • Have capacity to give consent to participate
Not Eligible

You will not qualify if you...

  • Did not proceed to surgery after CPET referral
  • Younger than 18 years
  • Do not have capacity to consent
  • Decline to consent
  • Have sensitivity or allergy to medical adhesives
  • Have fragile, erythematous, or broken skin at the site of PneumoRator attachment or any condition risking harm from the device or adhesive
  • Have implantable electronic medical devices such as pacemakers or nerve stimulators

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Southampon NHS Foundation Trust

Southampton, United Kingdom

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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