Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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)
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
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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