Actively Recruiting
EMUs Enhanced Monitoring Using Sensors After Surgery
Led by University of Edinburgh · Updated on 2026-02-10
1332
Participants Needed
17
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Edinburgh
Lead Sponsor
U
University of Birmingham
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to find out if wearable sensors can help detect early signs of health problems after major surgery. The study focuses on surgical patients who might become critically ill after their operations. It evaluates if continuous monitoring of vital signs like heart rate and oxygen levels using wearable devices can identify patient deterioration sooner than standard care. The study is observational and involves multiple countries including Benin, Ghana, Guatemala, India, Mexico, Nigeria, Rwanda, and the United Kingdom. Participants will wear wireless sensors on their chest and fingers before, during, and after surgery for up to 10 days. These sensors record vital signs continuously but do not affect patient care, as clinical teams will not access the data during the study. The first two stages of the study involved testing device usability with healthcare workers, while this third stage collects real-time sensor and clinical event data to explore links between physiological changes and patient complications. During the study, participants will have their vital signs monitored with wearable devices while also receiving standard clinical observations. Researchers will collect cardiovascular, respiratory, and temperature data alongside routine care information and clinical events. They will follow patients for 10 days of monitoring plus an additional 30-day follow-up to observe complications. The goal is to gather data to help design future algorithms for early detection of postoperative problems without changing current treatment practices.
CONDITIONS
Brief Title
EMUs: Enhanced Monitoring Using Sensors After Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years and older
- Undergoing elective or emergency major surgery with a planned skin incision of 5 cm or greater
- Willing and able to provide written informed consent
You will not qualify if you...
- Under 18 years of age
- Known or suspected allergy to adhesive dressings
- Obstetric patients
- Unwilling or unable to provide written informed consent
Research Team
E
Ewen Harrison
E
Eilidh Gunn
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