Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID05164744

Cardiac Magnetic Resonance for Tissue Characterization-Based Risk Stratification of Cardiopulmonary Symptoms, Effort Tolerance, and Prognosis Among COVID-19 Survivors

Led by Weill Medical College of Cornell University · Updated on 2026-01-22

510

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

W

Weill Medical College of Cornell University

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how cardiac MRI and echocardiogram imaging can help explain heart function and predict cardiopulmonary symptoms, physical effort tolerance, and outcomes in people who have survived COVID-19. The study focuses on a large and diverse group of at least 510 COVID-19 survivors, addressing the common long-term effects such as fatigue, shortness of breath, and reduced quality of life. Researchers want to identify the causes of lasting heart and lung symptoms to guide future treatments. Participants will undergo diagnostic tests including cardiac MRI, echocardiogram, a 6-minute walk test, and symptom questionnaires. These assessments will happen at specific follow-up times: initially more than 3 months after COVID-19 diagnosis, and again between 12 to 36 months later. The study will use advanced imaging techniques to assess heart and lung injury, tissue changes like fibrosis and edema, and blood oxygenation. During the study, participants will have their heart and lung imaging results analyzed alongside quality of life surveys, exercise tolerance tests, and clinical follow-up. The main outcomes measured include heart tissue changes, lung abnormalities, blood oxygen levels, quality of life scores, and physical effort capacity. The results will help clarify the impact of COVID-19 on heart function and guide prognosis and treatment strategies over time. Participants may be followed for up to 36 months after their first study visit.

CONDITIONS

Brief Title

Cardiac Magnetic Resonance Tissue Characterization in COVID-19 Survivors

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Emergency room visit or hospitalization with confirmed COVID-19 infection by PCR test
  • Presence of at least one symptom such as shortness of breath, cough, swallowing difficulty, runny nose, diarrhea, nausea, vomiting, muscle pain, fever, or fainting
Not Eligible

You will not qualify if you...

  • Contraindications to cardiac MRI such as incompatible pacemaker or defibrillator
  • Known allergy to gadolinium contrast or kidney function with eGFR less than 30 ml/min/1.73m2
  • Unable to provide informed consent due to cognitive impairment
  • Life expectancy less than 12 months from unrelated conditions like cancer
  • Known or suspected pregnancy based on screening surveys

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Day of first study visit, more than 3 months post COVID-19 infection

Participants undergo cardiac MRI, echocardiogram, 6-minute walk test, and complete questionnaires to assess heart and lung health as well as quality of life and effort tolerance.

1 visit (in-person)

Long-term Monitoring

Duration - 12 to 36 months after first study visit

Participants are followed up with repeat cardiac MRI, echocardiogram, 6-minute walk test, and questionnaires to monitor heart tissue changes, symptoms, and clinical outcomes over time.

1 to 2 visits depending on assessments

Trial Site Locations

Total: 3 locations

1

New York Presbyterian-Brooklyn Methodist Hospital

Brooklyn, New York, United States, 11215-3609

Actively Recruiting

2

New York Presbyterian Queens

New York, New York, United States, 10021

Actively Recruiting

3

Weill Cornell Medicine/New-York Presbyterian Hospital

New York, New York, United States, 10021

Actively Recruiting

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Research Team

E

Elizabeth Manowitz, BS

M

Mahniz Reza, BA

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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