Establishing a Non-invasive Method to Measure Your Heart's Performance

NCT02240979 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2019-05-14

No results posted yet for this study

Summary

The purpose of the study is to evaluate a new way to examine cardiac function, using software developed at Caltech. The experimental device is software loaded on an iPhone. The iPhone is used to capture a pulse (waveform) by simply placing the iPhone lightly over the neck where the carotid pulse can be felt. In this study the information collected from the iPhone app is compared to cardiac function data obtained from the current gold standard for measuring cardiac function, cardiac magnetic resonance imaging (MRI). Subjects referred from cardiologists will also generally have echocardiography information available for comparison with the iPhone app. For the study, subjects will have completely non-invasive studies done in one setting: The iPhone app to capture the waveforms (over carotid and radial (wrist) arteries), tonometry (another non-invasive method using a modified stethoscope), standard pulse oximetry, followed by a 30 minute MRI examination of the heart. A second complete study will be done about 6 months after the first. The complete study session takes about 1.5 hours.

Conditions

Interventions

DEVICE

cardiac MRI

cardiac MRI

Sponsors & Collaborators

  • University of Southern California

    collaborator OTHER
  • California Institute of Technology

    collaborator OTHER
  • Marie Csete MD, PhD

    lead OTHER

Principal Investigators

  • Marie Csete, MD, PhD · Avicena LLC

  • Niema Pahlevan, PhD · University of Southern California

Eligibility

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

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2019-05-31
Completion
2019-05-31

Countries

  • United States

Study Locations

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Entities

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 NCT02240979 on ClinicalTrials.gov