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Comparison Study of Non-invasive Measurement of Blood Pressure and Cardiac Output During Stress Echocardiography

NCT02422342 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2019-02-22

No results posted yet for this study

Summary

The objectives of the clinical trial is to validate hemodynamic parameters (Blood pressure and Cardiac Output) generated by an application coupled with an off-the-shelf pulse oximeter. The validation will be done by comparing the generated information to data gathered while performing Stress Echocardiography. The first phase of the study will be done on 10 patients undergoing a Stress Echocardiography test at the cardiology department at Meir Hospital

Conditions

  • High Cardiac Output
  • Low Cardiac Output

Interventions

DEVICE

Pulse Oximeter CMS50FW (Contec Medical)

The patients will be wearing the pulse oximeter during the test period (20-30 minutes). The data from the oximeter will be sent by Bluetooth to the mobile application

Sponsors & Collaborators

  • HeartBeat Technologies LTD

    lead INDUSTRY

Principal Investigators

  • Yoram Neuman, MD · Meir Health Facility

Eligibility

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

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2019-12-31
Completion
2019-12-31

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 NCT02422342 on ClinicalTrials.gov