- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT06103123
Myokardit och/eller perikardit efter mRNA COVID-19 VACCination National Surveillance Study (MYCOVACC)
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.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Beräknad)
Kontakter och platser
Studiekontakt
- Namn: Jenny Petterson, MSc
- Telefonnummer: 604-875-5104
- E-post: jenny.petterson@vch.ca
Studera Kontakt Backup
- Namn: Naomi Uchida, RN
- Telefonnummer: 604-875-5324
- E-post: naomi-uchida@ubc.ca
Studieorter
-
-
British Columbia
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Vancouver, British Columbia, Kanada, V5Z 1M9
- Rekrytering
- Vancouver General Hospital
-
Kontakt:
- Jenny Petterson, MSc
- Telefonnummer: 604 - 875 - 5104
- E-post: jenny.petterson@vch.ca
-
Huvudutredare:
- Nathaniel Hawkins, MD
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Patients who have suffered or are suffering from 1) COVID-19 infection associated myocarditis, 2) COVID-19 infection associated pericarditis, 3) COVID-19 vaccine associated myocarditis, 4) COVID-19 vaccine associated pericarditis, 5) Alternative etiology myocarditis, 6) Alternative etiology pericarditis
Definition of myocarditis and pericarditis follows standard clinical definition as outlined in "Brighton Collaboration myocarditis case definition and levels of diagnostic certainty 1,2 and 3"
Beskrivning
Inclusion Criteria:
-
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
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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
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No alternative cause of presentation. e.g. infectious or autoimmune myocarditis.
-
-
Inclusion criteria for COVID-19 associated myocarditis/pericarditis
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COVID-19 infection within the previous 42 days.
AND
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Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis.
AND
-
No alternative cause of presentation.
-
Inclusion criteria alternative etiology myocarditis.
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Myocarditis/pericarditis as per Brighton Criteria for vaccine associated myocarditis/pericarditis.
AND
-
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.
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: COHORT
- Tidsperspektiv: PROSPECTIVE
Kohorter och interventioner
Grupp / Kohort |
Intervention / Behandling |
|---|---|
|
mRNA COVID-19 vaccine associated myocarditis
Participants who had developed myocarditis within 42 days of getting a mRNA COVID-19 vaccine |
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 |
|
mRNA COVID-19 vaccine associated pericarditis
Participants who had developed pericarditis within 42 days of getting a mRNA COVID-19 vaccine |
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 |
|
COVID-19 infection associated myocarditis
Participants who had developed myocarditis within 42 days of being infected with the SARS-COV-2 virus |
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 |
|
COVID-19 infection associated pericarditis
Participants who had developed pericarditis within 42 days of being infected with the SARS-COV-2 virus |
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 |
|
Alternative etiology myocarditis
Any participants with myocarditis that is not associated with the mRNA COVID-19 vaccine or SARS-COV-2 viral infection |
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 |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
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)
Tidsram: From date of vaccination and up to 3 years
|
Including any of:
|
From date of vaccination and up to 3 years
|
|
Recovery of cardiac function in patients with previously documented abnormal cardiac function
Tidsram: Through study completion, an average of 3 years
|
Patients with Left Ventricular Ejection Fraction (LVEF)<55% during anytime at baseline, with LVEF increase by 5% from worst baseline measurement |
Through study completion, an average of 3 years
|
|
Quality of life using validated instruments at baseline, 3 months, 12 months, and annually
Tidsram: Through study completion, an average of 3 years
|
Quality of life: EQ-5D-5L questionnaire for adults or EQ-5D-Y questionnaire for children. |
Through study completion, an average of 3 years
|
|
Depression and anxiety using validated instruments at baseline, 3 months, 12 months, and annually
Tidsram: Through study completion, an average of 3 years
|
Depression and anxiety data: PHQ-9 and GAD-7. |
Through study completion, an average of 3 years
|
|
Physical activity using validated instruments at baseline, 3 months, 12 months, and annually
Tidsram: Through study completion, an average of 3 years
|
Physical activity: International Activity Questionnaire. |
Through study completion, an average of 3 years
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Individuella komponenter av primärt sammansatt effektmått 30 dagar och 42 dagar efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
|
Frekvens av förmaksarytmier efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
|
Frekvens av alla orsaker och kardiovaskulär dödlighet efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
|
Frekvens av alla orsaker och kardiovaskulär sjukhusvistelse efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
|
Frekvens för återfall av myokardit/perikardit efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
|
Frekvens av sammandragande perikardit efter mRNA COVID-19-vaccination?
Tidsram: Från vaccinationsdatum i upp till tre år
|
Från vaccinationsdatum i upp till tre år
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Nathaniel Hawkins, MD, Vancouver General Hospital
Publikationer och användbara länkar
Användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Hjärt-kärlsjukdomar
- Hjärtsjukdom
- Kardiomyopatier
- Myokardit
- Perikardit
- Diagnostiska tekniker och procedurer
- Diagnos
- Miljö och folkhälsa
- Fysiska fenomen
- Tomografi
- Diagnostisk avbildning
- Miljö
- Ekologiska och miljömässiga fenomen
- Biologiska fenomen
- Geologiska fenomen
- Magnetisk resonansavbildning
- Grottor
Andra studie-ID-nummer
- MYCOVACC
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