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

NCT ID: NCT02422342

Last Updated: 2019-02-22

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 50 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-04-30
• Study Completion Date: 2019-12-31

Brief 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

Detailed Description

The HeartBeat system combines an FDA/CE approved watch-like Pulse Oximeter for acquiring the data and an android software application that serves as the Hemodynamic calculator. The application performs POST-PROCESSING of the PhotoPlethismoGraphic (PPG) signal (Normally the PPG signal in Pulse Oximeters is used only to compute heart rate and SpO2). The raw data is transferred from the watch oximeter to the smartphone using a standard Bluetooth protocol.

The Post-processing uses wavelet signal processing to estimate and display certain Hemodynamic parameters like Blood Pressure (BP) and Cardiac Output (CO) in a continuous and graphical way on a standard Android device. In addition to the standard heart rate and SpO2, the application displays the measured PPG signal and estimated continues BP and CO.

HeartBeat is the only device that can non-invasively estimate Continuous BP and its Cardiac Output component and the resistance component in a mobile wearable device. Differentiating between these 2 components can play a major role in helping the doctor to understand the effect of cardiovascular medications and Lifestyle interventions.

The trial will compare blood pressure and cardiac output parameters measured during Stress Echocardiography using an echo cardiograph and standard sphygmomanometer to the parameters generated by the application.

Trial goals

• Feasibility tests for the HeartBeat application as a tool for monitoring BP and CO changes over time
• Compare BP and CO parameters generated by the applications to the ones measured by standard non-invasive equipment during a Stress Echocardiography
• Calculate additional parameters such as stroke volume, systematic vascular resistance and cardiac index

Conditions

High Cardiac Output; Low Cardiac Output

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

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

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Patients referred to an Stress Echocardiography test for cardiac diagnostics
• Male and Female
• Between 18 to 90 years old

Exclusion Criteria

• Under the age of 18 or over 90 years old
• Patients in Shock
• Patients with Moderate or Severe valvular disease
• Patients with severe sepsis
• Inadequate jurisprudence patients
• Patients supported by Amines

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

HeartBeat Technologies LTD

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yoram Neuman, MD

Role: PRINCIPAL_INVESTIGATOR

Meir Health Facility

Locations

Meir Health Center

Kfar Saba, , Israel

Countries

Israel

Other Identifiers

HeartBeat_V2.0_SE

Identifier Type: -

Identifier Source: org_study_id