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uSing Wearable TEchnology to Predict Perioperative High-riSk Patient Outcomes

NCT03328039 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2019-05-20

No results posted yet for this study

Summary

This is an observational, non-interventional study to assess the equivalence of wearable monitors with formal CPET testing for the prediction of physiological reserve before major surgery.

Conditions

  • Perioperative Care

Interventions

DEVICE

Garmin wearable device

Physiological data capture only

Sponsors & Collaborators

  • Cardiff and Vale University Health Board

    collaborator OTHER_GOV

  • Cardiff University

    lead OTHER

Principal Investigators

  • Matt Morgan, PhD · Cardiff University

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2019-01-01
Completion
2019-01-01

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03328039 on ClinicalTrials.gov