Validation of Ventriject Determined Maximal Oxygen Uptake

NCT03504306 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2019-01-15

No results posted yet for this study

Summary

This study aims to validate the use of the Ventriject product to estimate VO2 max, through a non-physically active test using ECG, echoseismography and echosonography.

Conditions

  • Healthy

Interventions

OTHER

Ventriject validation

comparing measurements from echocardiography, echoseismography to measurements of maximal oxygen uptake

Sponsors & Collaborators

  • University of Copenhagen

    lead OTHER

Principal Investigators

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-23
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Denmark

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 NCT03504306 on ClinicalTrials.gov