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Comparison of the Non-invasive Biobeat Device With an Invasive Arterial Line

NCT03603860 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 18

Last updated 2020-07-09

No results posted yet for this study

Summary

In this clinical study the investigators will compare blood pressure measurements obtained using the non-invasive, continuous and wireless Biobeat monitoring device (a wrist watch or a patch configuration) to an invasive arterial line (radial or femoral) in 30 patients immediately after cardiac surgery, at the intensive care unit.

Conditions

  • Blood Pressure
  • Heart Diseases

Interventions

DEVICE

Non-invasive monitoring

Comparing blood pressure measurement using the Biobeat non-invasive monitor to arterial line

Sponsors & Collaborators

  • The Baruch Padeh Medical Center, Poriya

    collaborator OTHER_GOV

  • Biobeat Technologies Ltd.

    lead INDUSTRY

Principal Investigators

  • Erez Kachel, MD · The Baruch Padeh Medical Center, Poriya, Israel

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-05
Primary Completion
2020-02-05
Completion
2020-03-05

Countries

  • Israel

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 NCT03603860 on ClinicalTrials.gov