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

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test, Other
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Inclusion criteria for vaccine associated myocarditis/pericarditis.

∙ COVID-19 vaccination within previous 42 days. AND

‣ 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

‣ At least one of the following objective findings (Brighton Criteria case definitions, Appendices 1 to 5):

⁃ Histopathologic examination of myocardial tissue (autopsy or endomyocardial biopsy) showed myocardial inflammation.

• Elevated myocardial biomarker (Troponin T, Troponin I, or CK-MB).

• Cardiac MRI abnormality.

• Echocardiographic abnormality.

• New or worsening arrhythmia on electrocardiogram, Holter monitor, or telemetry.

• Elevated inflammation biomarkers: erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), hs-CRP, or D-Dimer.

• Physical examination pericardial friction rub or pulsus paradoxus.

• Pericardial fluid or inflammation by imaging (echo, MRI, or CT).

• Enlarged heart on chest radiograph.

∙ AND

‣ No alternative cause of presentation. e.g. infectious or autoimmune myocarditis.

• Inclusion criteria for COVID-19 associated myocarditis/pericarditis

∙ COVID-19 infection within the previous 42 days.

∙ AND

‣ Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis.

∙ AND

‣ No alternative cause of presentation.

⁃ Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis.

⁃ AND

⁃ No alternative cause of presentation.

Locations
Other Locations
Canada
Vancouver General Hospital
RECRUITING
Vancouver
Contact Information
Primary
Jenny Petterson, MSc
jenny.petterson@vch.ca
604-875-5104
Backup
Naomi Uchida, RN
naomi-uchida@ubc.ca
604-875-5324
Time Frame
Start Date: 2023-04-23
Estimated Completion Date: 2025-04-23
Participants
Target number of participants: 500
Treatments
mRNA COVID-19 vaccine associated myocarditis
Participants who had developed myocarditis within 42 days of getting a mRNA COVID-19 vaccine
mRNA COVID-19 vaccine associated pericarditis
Participants who had developed pericarditis within 42 days of getting a mRNA COVID-19 vaccine
COVID-19 infection associated myocarditis
Participants who had developed myocarditis within 42 days of being infected with the SARS-COV-2 virus
COVID-19 infection associated pericarditis
Participants who had developed pericarditis within 42 days of being infected with the SARS-COV-2 virus
Alternative etiology myocarditis
Any participants with myocarditis that is not associated with the mRNA COVID-19 vaccine or SARS-COV-2 viral infection
Sponsors
Leads: Cardiology Research UBC

This content was sourced from clinicaltrials.gov