Actively Recruiting

Age: 18Years +
All Genders
ID06565559

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 10 days from device application

Participants wear a wireless sensor device before, during, and after their surgery while receiving standard care. Sensor data is collected continuously but not used to make clinical decisions.

Continuous monitoring during hospital stay for up to 10 days

Long-term Monitoring

Duration - 30 days after sensor monitoring ends

Participants are followed up for 30 days after sensor monitoring to assess clinical outcomes and complications.

1 follow-up visit

Trial Site Locations

Total: 17 locations

1

Hopital de Zone Atlantique Ouidah

Ouidah, Atlantique Department, Benin

Actively Recruiting

2

Centre Hospitalier Universitaire Departemental Borgou-Alibori

Parakou, Borgou Department, Benin

Actively Recruiting

3

Centre Hospitalier Universitaire Mere Enfant Lagune

Cotonou, Littoral Department, Benin

Actively Recruiting

4

Centre Hospitalier Universitaire et Departemental Oueme Plateau

Porto-Novo, Oeume, Benin

Actively Recruiting

5

Berekum Holy Family Hospital

Berekum, Berekum East, Ghana

Actively Recruiting

6

Techiman Holy Family Hospital

Techiman, Bono East, Ghana

Actively Recruiting

7

Tamale Teaching Hospital

Tamale, Ghana

Actively Recruiting

8

Hospital General San Juan de Dios

Guatemala City, Guatemala

Actively Recruiting

9

Lady Willingdon Hospital

Manali, Himachal Pradesh, India

Actively Recruiting

10

Padhar Hospital

Pādhar, Madhya Pradesh, India

Actively Recruiting

11

Christian Medical College and Hospital

Ludhiana, Punjab, India

Actively Recruiting

12

Hospital Español de Veracruz

Veracruz, Mexico

Actively Recruiting

13

Obafemi Awolowo University Teaching Hospital Complex

Ife, Nigeria

Not Yet Recruiting

14

Lagos State University Teaching Hospital

Ikeja, Nigeria

Not Yet Recruiting

15

Lagos University Teaching Hospital

Lagos, Nigeria

Actively Recruiting

16

University Teaching Hospital of Rwanda

Kigali, Rwanda

Not Yet Recruiting

17

Royal Infirmary of Edinburgh

Edinburgh, United Kingdom, EH16 4SA

Active, Not Recruiting

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Research Team

E

Ewen Harrison

E

Eilidh Gunn

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Continuous physiological monitoring for the detection of postoperative deterioration: a protocol for a multistage, multicentre, international, prospective cohort study.

Afra Jiwa, Malcolm M Cameron, Adesoji O Ademuyiwa...

https://pubmed.ncbi.nlm.nih.gov/41057181