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COvid-19 LongitUdinal Multiethnic BioImaging Assessment of CARDiovascular Sequelae Registry

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04661657
Enrollment
52
Registered
2020-12-10
Start date
2020-12-28
Completion date
2022-01-22
Last updated
2022-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Cardiac Disease, Cardiac Arrhythmia, Myocarditis, Left Ventricular Dysfunction

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.

Interventions

Subjects will undergo TTE imaging.

OTHERCardiovascular Magnetic Resonance (CMR) Imaging

Subjects will undergo CMR Imaging using a gadolinium based contrast agent (GBCA).

Sponsors

GE Healthcare
CollaboratorINDUSTRY
Columbia University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Percentage of myocardium demonstrating late gadolinium enhancementUp to 2 hoursPercentage of myocardium demonstrating late gadolinium enhancement by cardiac magnetic resonance (CMR) imaging, determined using Circle cvi42 software.
Extracellular Volume (ECV) FractionUp to 2 hoursExtracellular volume fraction measured by CMR imaging. ECV determined using Circle cvi42 software and using formula ECV = (1-hematocrit) × (Δ(1/T1myocardium)/Δ(1/T1blood)).
Left Ventricular Ejection FractionUp to 2 hoursLeft ventricular ejection fraction (percent ejection fraction) by CMR imaging and determined using Circle cvi42 software.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026