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Myocardial Injury and Outcomes Following COVID-19 Vaccination (MYOVAX Study) (MYOVAX)

Primary Purpose

Myocardial Injury, Myocarditis, COVID-19 Vaccination

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cardiac PET/MRI
Blood Biomarkers
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Myocardial Injury

Eligibility Criteria

17 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age ≥ 17 years (both Cohort A and B)
  2. Received at least one dose of a COVID-19 vaccine in the past 6 months (both Cohort A and B)
  3. Developed new clinical signs or symptoms suggestive of myocarditis/myocardial injury within one month of COVID vaccine administration without other known cause (Cohort A, only)

Exclusion Criteria:

  1. Contraindications to cardiac PET/MRI
  2. Current history of COVID-19

Sites / Locations

  • University Health NetworkRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Cohort A - Symptomatic

Cohort B - Asymptomatic

Arm Description

Those with clinical findings suggestive of myocarditis/myocardial injury after COVID-19 vaccination

Those without signs or symptoms suggestive of myocarditis after COVID-19 vaccination

Outcomes

Primary Outcome Measures

Prevalence of myocardial inflammation on PET/MRI
The prevalence of myocardial inflammation on PET/MRI will be compared between symptomatic and asymptomatic patients

Secondary Outcome Measures

Major adverse cardiac events (MACE)
Defined as a composite of: Arrhythmias - new atrial or ventricular arrhythmia Acute coronary syndrome Acute myocardial infarction Unstable angina requiring revascularization (PCI or CABG) Heart failure hospitalization Cardiovascular death
Left ventricular dysfunction
Defined as Left Ventricular Ejection Fraction (LVEF) < lower limit of normal on MRI
Myocardial edema
Defined as high T2 > upper limit of normal on MRI

Full Information

First Posted
June 29, 2021
Last Updated
November 1, 2022
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT04967807
Brief Title
Myocardial Injury and Outcomes Following COVID-19 Vaccination (MYOVAX Study)
Acronym
MYOVAX
Official Title
Myocardial Injury and Outcomes Following COVID-19 Vaccination (MYOVAX Study)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 5, 2021 (Actual)
Primary Completion Date
August 5, 2023 (Anticipated)
Study Completion Date
August 5, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study will focus on cardiac blood and imaging biomarkers to facilitate early recognition of patients at risk for myocardial injury after COVID-19 vaccination. Ultimately, the intention is to identify patients at risk, reduce adverse events, and determine the need for longer-term follow-up in patients with myocardial injury after vaccination.
Detailed Description
Coronavirus disease 2019 (COVID-19) vaccination frequently leads to minor side effects that may be more intense after the second dose, including fatigue and pain. However, there are emerging reports of more serious side effects in a minority of patients including myocarditis. Given the recent introduction of COVID-19 vaccination, there is limited understanding of: (i) prevalence and pattern of myocardial injury post vaccination, (ii) the risk factors for myocardial injury and adverse cardiac events post vaccination, and (iii) imaging and blood biomarkers for early recognition of patients at risk of adverse outcomes. This study will address the above-mentioned knowledge gaps by focusing on patients who have received at least one dose of a COVID-19 vaccine. The study will focus on cardiac blood and imaging biomarkers to facilitate early recognition of patients at risk for myocardial injury after COVID-19 vaccination. Ultimately, the intention is to identify patients at risk, reduce adverse events, and determine the need for longer-term follow-up in patients with myocardial injury after vaccination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Injury, Myocarditis, COVID-19 Vaccination, SARS-CoV-2, Cardiac MRI

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study population will include 2 cohorts of patients post COVID-19 vaccination. Cohort A) symptomatic patients with clinical signs or symptoms suggestive of myocardial injury and Cohort B) asymptomatic patients without symptoms suggestive of myocardial injury who have had prior cardiac MRI.
Masking
None (Open Label)
Masking Description
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cohort A - Symptomatic
Arm Type
Other
Arm Description
Those with clinical findings suggestive of myocarditis/myocardial injury after COVID-19 vaccination
Arm Title
Cohort B - Asymptomatic
Arm Type
Other
Arm Description
Those without signs or symptoms suggestive of myocarditis after COVID-19 vaccination
Intervention Type
Diagnostic Test
Intervention Name(s)
Cardiac PET/MRI
Intervention Description
An imaging technique that combines the strengths of both MRI and PET into one comprehensive study. This technique allows for detailed myocardial tissue characterization with MRI (including assessment of myocardial edema and fibrosis) and metabolic changes (including myocardial inflammation).
Intervention Type
Diagnostic Test
Intervention Name(s)
Blood Biomarkers
Intervention Description
Markers of cardiac damage, inflammation, circulating microRNA profiles, and COVID antibody levels will be evaluated in patients after COVID-19 vaccination.
Primary Outcome Measure Information:
Title
Prevalence of myocardial inflammation on PET/MRI
Description
The prevalence of myocardial inflammation on PET/MRI will be compared between symptomatic and asymptomatic patients
Time Frame
6months and 12months
Secondary Outcome Measure Information:
Title
Major adverse cardiac events (MACE)
Description
Defined as a composite of: Arrhythmias - new atrial or ventricular arrhythmia Acute coronary syndrome Acute myocardial infarction Unstable angina requiring revascularization (PCI or CABG) Heart failure hospitalization Cardiovascular death
Time Frame
6months and 12months
Title
Left ventricular dysfunction
Description
Defined as Left Ventricular Ejection Fraction (LVEF) < lower limit of normal on MRI
Time Frame
6months and 12months
Title
Myocardial edema
Description
Defined as high T2 > upper limit of normal on MRI
Time Frame
6months and 12months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 17 years (both Cohort A and B) Received at least one dose of a COVID-19 vaccine in the past 6 months (both Cohort A and B) Developed new clinical signs or symptoms suggestive of myocarditis/myocardial injury within one month of COVID vaccine administration without other known cause (Cohort A, only) Exclusion Criteria: Contraindications to cardiac PET/MRI Current history of COVID-19
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kate Hanneman, MD
Phone
416-323-6400
Ext
5521
Email
Kate.Hannaman@uhn.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Paaladinesh Thavendiranathan, MD
Phone
416-340-5326
Email
Dinesh.Thavendiranathan@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kate Hanneman, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kate Hanneman, MD
Phone
416-323-6400
Ext
5521
Email
kate.hanneman@uhn.ca

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Myocardial Injury and Outcomes Following COVID-19 Vaccination (MYOVAX Study)

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