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MYocarditis and/or Pericarditis Following mRNA COVID-19 VACCination National Surveillance Study

MYocarditis and/or Pericarditis Following mRNA COVID-19 VACCination National Surveillance Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06103123
Acronym
MYCOVACC
Enrollment
500
Registered
2023-10-26
Start date
2023-04-23
Completion date
2025-04-23
Last updated
2023-10-26

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

Conditions

Myocarditis, Myocarditis Acute, Pericarditis, Pericarditis Acute

Brief summary

Myocarditis is inflammation of the heart muscle. Pericarditis is inflammation of the lining surrounding the heart muscle. Symptoms of these conditions can include pain in the chest and rapid or irregular heartbeat. There are many different causes for myocarditis and pericarditis including COVID-19 infection. The MYCOVACC study will identify patients using local screening strategies, including research communications, care provider referrals, and medical record review. The retrospective component of the study will collect information about patients suffering from vaccine associated myopericarditis and COVID-19 associated myopericarditis. Consenting patients will then be prospectively followed according to standard of care protocols. The main objectives of MYCOVACC are to describe the rate of major adverse cardiovascular events, functional outcomes including quality of life, and myocardial recovery through imaging.

Interventions

DIAGNOSTIC_TESTStand of care ECG, Holter, MRI, ECHO, Quality of life questionnaire

Stand of care ECG, Holter, MRI, ECHO, Quality of life questionnaire will be used to follow the clinical outcomes and patient reported outcomes to assess for study objectives

OTHERBaseline Quality of Life questionnaire

Only baseline quality of life questionnaires will be utilized in the alternative etiology myocarditis cohort as they will not be followed up in the study

Sponsors

Cardiology Research UBC
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Inclusion criteria for vaccine associated myocarditis/pericarditis. 1. COVID-19 vaccination within previous 42 days. AND 2. At least one cardiac symptom of suspected myocarditis/pericarditis (Appendix 5). OR At least two non-specific symptoms (Appendix 5). OR In infants and young children, at least two non-specific pediatric symptoms (Appendix 5). OR No symptoms, but abnormal histopathology or a combination of abnormal cardiac biomarkers with abnormal cardiac imaging (echo or MRI). AND 3. At least one of the following objective findings (Brighton Criteria case definitions, Appendices 1 to 5): 1. Histopathologic examination of myocardial tissue (autopsy or endomyocardial biopsy) showed myocardial inflammation. 2. Elevated myocardial biomarker (Troponin T, Troponin I, or CK-MB). 3. Cardiac MRI abnormality. 4. Echocardiographic abnormality. 5. New or worsening arrhythmia on electrocardiogram, Holter monitor, or telemetry. 6. Elevated inflammation biomarkers: erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), hs-CRP, or D-Dimer. 7. Physical examination pericardial friction rub or pulsus paradoxus. 8. Pericardial fluid or inflammation by imaging (echo, MRI, or CT). 9. Enlarged heart on chest radiograph. AND 4. No alternative cause of presentation. e.g. infectious or autoimmune myocarditis. * Inclusion criteria for COVID-19 associated myocarditis/pericarditis 1. COVID-19 infection within the previous 42 days. AND 2. Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis. AND 3. No alternative cause of presentation. Inclusion criteria alternative etiology myocarditis. 1. Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis. AND 2. No alternative cause of presentation.

Exclusion criteria

* For prospective invitation and follow-up, inability to provide informed consent. Consent will be sought from patients or their authorised substitute decision maker. * Patients not fulfilling Brighton Criteria levels 1-3 will be excluded if they are level 4 (insufficient evidence for myocarditis) or Level 5 (not myocarditis) or have an alternative diagnosis such as myocardial infarction.

Design outcomes

Primary

MeasureTime frameDescription
Composite Major Adverse Cardiac Event (MACE) at 30 days post vaccination (preferred by cardiovascular community) and at 42 days post vaccination (preferred by vaccine monitoring investigators)From date of vaccination and up to 3 yearsIncluding any of: * Death from any cause. * Ventricular arrhythmia (ventricular fibrillation or ventricular tachycardia). * Heart block (type II or type III block). * Heart failure (national guideline criteria). * Left ventricular systolic dysfunction (left ventricular ejection fraction \[LVEF\] \<55%). * Cardiac tamponade.
Recovery of cardiac function in patients with previously documented abnormal cardiac functionThrough study completion, an average of 3 yearsPatients with Left Ventricular Ejection Fraction (LVEF)\<55% during anytime at baseline, with LVEF increase by 5% from worst baseline measurement
Quality of life using validated instruments at baseline, 3 months, 12 months, and annuallyThrough study completion, an average of 3 yearsQuality of life: EQ-5D-5L questionnaire for adults or EQ-5D-Y questionnaire for children.
Depression and anxiety using validated instruments at baseline, 3 months, 12 months, and annuallyThrough study completion, an average of 3 yearsDepression and anxiety data: PHQ-9 and GAD-7.
Physical activity using validated instruments at baseline, 3 months, 12 months, and annuallyThrough study completion, an average of 3 yearsPhysical activity: International Activity Questionnaire.

Secondary

MeasureTime frame
Individual components of primary composite endpoint at 30 days and 42 days post mRNA COVID-19 vaccination?From date of vaccination for up to three years
Rate of constrictive pericarditis after mRNA COVID-19 vaccination?From date of vaccination for up to three years
Rate of atrial arrhythmias after mRNA COVID-19 vaccination?From date of vaccination for up to three years
Rate of all-cause and cardiovascular mortality after mRNA COVID-19 vaccination?From date of vaccination for up to three years
Rate of all-cause and cardiovascular hospitalization after mRNA COVID-19 vaccination?From date of vaccination for up to three years
Rate of recurrence of myocarditis/pericarditis after mRNA COVID-19 vaccination?From date of vaccination for up to three years

Countries

Canada

Contacts

Primary ContactJenny Petterson, MSc
jenny.petterson@vch.ca604-875-5104
Backup ContactNaomi Uchida, RN
naomi-uchida@ubc.ca604-875-5324

Outcome results

None listed

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