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Clinical Trials/NCT04661657
NCT04661657CompletedNot Applicable

COvid-19 LongitUdinal Multiethnic BioImaging Assessment of CARDiovascular Sequelae (COLUMBIA CARDS) Registry

Columbia University1 site in 1 country52 target enrollmentStarted: December 28, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
1
Primary Endpoint
Percentage of myocardium demonstrating late gadolinium enhancement

Study Overview

Brief Summary

COLUMBIA CARDS is a pilot study to understand how COVID-19 affects the heart. It is known that COVID-19 can affect the heart in different ways. COLUMBIA CARDS is studying why some COVID-19 survivors develop clinical conditions such as heart inflammation, fluid buildup, blood clots, and other cardiac problems during or after their COVID-19 illness, and why other ones do not. In this study, we will use cardiovascular magnetic resonance (CMR) and transthoracic echocardiography (TTE) to better understand the impact of COVID-19 on the heart.

Detailed Description

This is a pilot study aiming to collect preliminary data on cardiac imaging (CMR and TTE) in outpatients who recovered from COVID-19.

CMR offers the unique ability to comprehensively characterize myocardial tissue and assess the heart's structure and function, through a variety of complementary imaging techniques using different pulse sequences. The investigators propose to provide a multi-sequence CMR evaluation of a spectrum of convalescent COVID-19 patients, compare COVID-19 survivors to controls, and study the relationships between myocardial characteristics by CMR and echocardiography and health outcomes, and how these are modulated through patient characteristics, and clinical characteristics of COVID-19 illness. Broadly, this myocardial characterization will not just provide diagnosis but serve as a potentially powerful tool for risk stratification, therapeutic decision making, and monitoring response to therapies in COVID-19 survivors.

Transthoracic echocardiography (TTE) is the most widely used imaging technique for the assessment of cardiac morphology and function. While its capability for myocardial tissue characterization is inferior to that of CMR, TTE provides several advantages that make it an ideal complement to CMR for the assessment of cardiac involvement in COVID-19 patients. TTE offers a rapid noninvasive evaluation of myocardial and valvular function, in addition to the assessment of other cardiac abnormalities of interest (such as presence and amount of pericardial effusion) and important hemodynamic variables (noninvasive estimation of pulmonary pressures is an example). TTE is easily performed and reproducible, and does not involve the use of radiations or contrast agents, which allows the performance of repeat evaluations to assess serial changes over time in the cardiac parameters of interest.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Convalescent COVID-19 patient
  • If COVID-19 patient, at least 4 weeks after beginning of symptoms, and at least 2 weeks after hospital discharge if had been hospitalized.
  • Control patients who have had a negative COVID-19 screening without prior positive tests.
  • Willingness to undergo Clariscan-enhanced CMR scan.
  • Ability to hold breath for 15 seconds.
  • Willingness to give informed consent.
  • Greater than or equal to 18 years of Age.

Exclusion Criteria

  • Subjects who are Pregnant or nursing
  • Severe valvular heart disease
  • History of congestive heart failure preceding COVID-19
  • History of obstructive coronary artery disease with known stenosis >70% or fractional flow reserve < 0.8
  • Contraindication to MRI
  • Known allergy to gadoterate
  • Estimated glomerular filtration rate <30 ml/min/1.73m2
  • History of receiving more than 2 doses of a gadolinium-based contrast agent
  • Subject is of prisoner status

Outcomes

Primary Outcomes

Percentage of myocardium demonstrating late gadolinium enhancement

Time Frame: Up to 2 hours

Percentage of myocardium demonstrating late gadolinium enhancement by cardiac magnetic resonance (CMR) imaging, determined using Circle cvi42 software.

Left Ventricular Ejection Fraction

Time Frame: Up to 2 hours

Left ventricular ejection fraction (percent ejection fraction) by CMR imaging and determined using Circle cvi42 software.

Extracellular Volume (ECV) Fraction

Time Frame: Up to 2 hours

Extracellular volume fraction measured by CMR imaging. ECV determined using Circle cvi42 software and using formula ECV = (1-hematocrit) × (Δ(1/T1myocardium)/Δ(1/T1blood)).

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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