Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Smart patches could predict Post-Surgery complications

NCT ID NCT06565559

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is testing whether wearable sensors on the chest and fingers can detect early signs of patient decline after major surgery. Over 1,300 adults in eight countries will wear the sensors before, during, and after their operation for up to 10 days. The data will be used to design algorithms that might one day alert doctors to complications sooner. For now, the sensor data is only being collected and analyzed—it does not change patient care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Wearable wireless sensor (chest and finger patches)
What this could lead to
If successful, this could lead to an early warning system that helps doctors spot complications sooner after surgery, potentially saving lives.
What could go wrong
This is an early-stage observational study—sensor data is not used to guide patient care yet. The algorithms developed may not work in real-world settings or may produce too many false alarms.

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.

Participants

About 1,332 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2024

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population are all patients undergoing a surgical procedure at the NIHR Global Health Research Unit on Global Surgery hubs/spoke hospitals in India, Nigeria, Ghana, Guatemala, Mexico, Rwanda, Benin and the United Kingdom that fit the eligibility criteria.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Participant Inclusion Criteria: * Adults 18 years and older. * Undergoing an elective or emergency major surgery procedure with a planned skin incision of 5 cm or greater. Any indication for surgery can exist, including benign, malignant, and trauma. * Willing and able to provide written informed consent. Participant Exclusion Criteria: * Those under the age of 18. * A documented or suspected allergy to adhesive dressings. * Obstetric patients * Unwilling or unable to provide written informed consent.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Inpatients are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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.

  1. The places running it

    16 sites in 7 countries. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Berekum Holy Family Hospital

    RECRUITING

    Berekum, Berekum East, Ghana

  • Centre Hospitalier Universitaire Departemental Borgou-Alibori

    RECRUITING

    Parakou, Borgou Department, Benin

  • Centre Hospitalier Universitaire Mere Enfant Lagune

    RECRUITING

    Cotonou, Littoral Department, Benin

  • Centre Hospitalier Universitaire et Departemental Oueme Plateau

    RECRUITING

    Porto-Novo, Oeume, Benin

  • Christian Medical College and Hospital

    RECRUITING

    Ludhiana, Punjab, India

  • Hopital de Zone Atlantique Ouidah

    RECRUITING

    Ouidah, Atlantique Department, Benin

  • Hospital Español de Veracruz

    RECRUITING

    Veracruz, Mexico

  • Hospital General San Juan de Dios

    RECRUITING

    Guatemala City, Guatemala

  • Lady Willingdon Hospital

    RECRUITING

    Manali, Himachal Pradesh, India

  • Lagos State University Teaching Hospital

    NOT_YET_RECRUITING

    Ikeja, Nigeria

  • Lagos University Teaching Hospital

    RECRUITING

    Lagos, Nigeria

  • Obafemi Awolowo University Teaching Hospital Complex

    NOT_YET_RECRUITING

    Ife, Nigeria

  • Padhar Hospital

    RECRUITING

    Pādhar, Madhya Pradesh, India

  • Royal Infirmary of Edinburgh

    ACTIVE_NOT_RECRUITING

    Edinburgh, EH16 4SA, United Kingdom

  • Tamale Teaching Hospital

    RECRUITING

    Tamale, Ghana

  • Techiman Holy Family Hospital

    RECRUITING

    Techiman, Bono East, Ghana

  • University Teaching Hospital of Rwanda

    NOT_YET_RECRUITING

    Kigali, Rwanda

More trials for these conditions

Other studies related to the condition(s) this trial covers.