Actively Recruiting

Age: 18Years +
All Genders
NCT07473687

Feasibility Study of Non-Contact Imaging-Based Physiological Monitoring in the Operating Room

Led by Taipei Veterans General Hospital, Taiwan · Updated on 2026-03-16

315

Participants Needed

1

Research Sites

233 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the feasibility and accuracy of a non-contact, camera-based physiological monitoring technology in a perioperative setting (including anesthesia induction, surgery, and recovery).Conventional vital sign monitoring tools-such as ECG leads, blood pressure cuffs, and pulse oximeters-require direct skin contact, which may pose risks of cross-infection or skin injury in vulnerable populations (e.g., newborns or elderly patients). This research utilizes remote Photoplethysmography (rPPG) technology to estimate vital signs, including heart rate, blood pressure, and blood oxygen saturation (SpO2), by analyzing facial video captured via standard camera devices (Logitech C930, iPhone 16 Pro Max, and Samsung Galaxy S24 Ultra).The primary goal is to assess the consistency and stability of this non-contact system compared to clinical gold-standard monitors (Masimo Root, SedLine O3, and Radical-7) during actual surgical procedures. The findings will serve as a foundation for developing non-invasive, supplementary monitoring tools in dynamic clinical environments.

CONDITIONS

Official Title

Feasibility Study of Non-Contact Imaging-Based Physiological Monitoring in the Operating Room

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged >18 years
  • Scheduled for surgery under general anesthesia
  • American Society of Anesthesiologists (ASA) Physical Status I, II, or III
Not Eligible

You will not qualify if you...

  • Patients aged <18 years
  • Pregnant patients
  • Patients whose facial images cannot be captured or recognized due to dressings, severe swelling, or trauma
  • Patients who refuse participation or have not signed consent
  • Patients deemed unsuitable by clinical physician or anesthesiologist

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

Department of Anesthesiology, Taipei Veterans General Hospital

Taipei, Taiwan, 11217

Actively Recruiting

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Research Team

H

Hui-Hsuan Ke

CONTACT

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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