Comprehensive Imaging Exam of Convalesced COVID-19 Patients
NCT ID: NCT05920616
Last Updated: 2025-06-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
NA
210 participants
INTERVENTIONAL
2020-10-14
2026-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Hospitalized
Participants who were hospitalized due to their COVID-19 illness.
Magnetic Resonance Imaging
Completion of Magnetic Resonance Imaging of the brain, heart, lungs, and liver with and without contrast.
Ultra-High Resolution Computed Tomography (CT) Scan
Completion of a high resolution CT scan of the lungs and high resolution CT of the coronary arteries.
Non-Hospitalized
Participants who had COVID-19 but did not require hospitalization secondary to their illness.
Magnetic Resonance Imaging
Completion of Magnetic Resonance Imaging of the brain, heart, lungs, and liver with and without contrast.
Ultra-High Resolution Computed Tomography (CT) Scan
Completion of a high resolution CT scan of the lungs and high resolution CT of the coronary arteries.
Interventions
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Magnetic Resonance Imaging
Completion of Magnetic Resonance Imaging of the brain, heart, lungs, and liver with and without contrast.
Ultra-High Resolution Computed Tomography (CT) Scan
Completion of a high resolution CT scan of the lungs and high resolution CT of the coronary arteries.
Eligibility Criteria
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Inclusion Criteria
* Diagnosed with COVID-19 at any point starting March 2020.
* Subgroup A: hospitalized due to COVID-19 infection
* Subgroup B: non-hospitalized
Exclusion Criteria
* Glomerular Filtration Rate (GFR) \<45 mL/min (using the Cockcroft-Gault formula)
* Pregnancy
* Internal electrical devices, such as cochlear implant, spinal cord stimulator, pacemaker, or defibrillator
* Atrial fibrillation, uncontrolled tachyarrhythmia or advanced atrioventricular block (2nd or 3rd degree) at time of imaging
* Evidence of severe symptomatic heart failure (NYHA Class III or IV) at the time of imaging
* Other acute illness
* Ongoing mechanical ventilation related to hospitalization for COVID-19 related illness
* Presence of any other history or condition that the investigator feels would be problematic
* Weight exceeding 300 lbs (MRI table weight restrictions)
* Severe claustrophobia
18 Years
ALL
No
Sponsors
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Canon Medical Systems, USA
INDUSTRY
Johns Hopkins University
OTHER
Responsible Party
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Principal Investigators
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Joao Lima, MD
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins School of Medicine
Locations
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Johns Hopkins School of Medicine
Baltimore, Maryland, United States
Countries
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Other Identifiers
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IRB00252436
Identifier Type: -
Identifier Source: org_study_id
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