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Myocarditis Post Vaccination or Multi System Inflammatory Syndrome

Consequences of Post BNT162b2 Vaccine Myocarditis and Multiple Inflammatory Syndrome Myocarditis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05288426
Acronym
MyoVax
Enrollment
150
Registered
2022-03-21
Start date
2021-11-01
Completion date
2025-12-01
Last updated
2022-03-21

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

Conditions

Myocarditis

Brief summary

BNT162b2 vaccine has become one of the most prevalent vaccines against the COVID-19 and is currently the main vaccine used in Israel. Since marketing and the beginning of use of the vaccine, we and others have reported. of the development of post vaccination myocarditis. In this study the investigators wish to explore the long term impact on 150 patients who have been diagnosed with myocarditis or multisystem inflammatory syndrome (MIS) in the year following their diagnosis of Myocarditis.

Detailed description

Aim of Study The primary aim of the study is to evaluate the impact of long term impact of myocarditis which has been developed secondary to Covid 19 vaccine or Covid 19 infection. The primary end points of the study will be functional evaluations of the patients using clinical evaluation that includes questionnaires, ECG findings, evaluation of the systolic and diastolic function of the heart using echocardiogram or cardiac MRI, laboratory tests including troponin, CPK, CRP, Pro-BNP, and cytokines/chemokines. Methods In this prospective study patients will be recruited from health care providers The selected patients will come to Hadassah hospital within 6 and 12 months after they have been diagnosed with myocarditis. Upon the patients arrival they will sign the informed consent, the investigators will draw blood tests and the participants will perform an echocardiogram according to the special protocol and will perform cardiac- MRI according to the myocarditis protocol. Patients will fulfill health questionnaires. that may include 36 Health Survey Questionnaire (SF-36); Scores on the European Quality of Life-5 Dimensions (EQ-5D) survey, which is also health-related quality of life score; the Scores on the European Quality of Life Visual Analogue Scale (EQ-VAS); Kansas City Cardiomyopathy Questionnaire (KCCQ). the Investigators will obtain blood samples from all the patients: complete blood count, c- reactive protein, troponin, CPK, Pro-BNP, liver and kidney functions, magnesium and cytokines. In addition, all participants will undergo echocardiogram test to evaluate their systolic and diastolic function of the heart. Ethical Considerations The study poses no danger to the participants. It has the potential to improve the understanding of the impact myocarditis post COVID-19 MRNA vaccine on the quality of life of those patients and provide a descent follow-up for the participant. Any participant will sign on informed consent form.

Interventions

OTHERNo intervention

This is an observational study, with no intervention.

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult males and females. * Minors male and female. Diagnosed as myocarditis: * Evidence of myocarditis on biopsy or increased biomarkers of myocardial injury (TNI and CK-MB and BNP or NT-pro-BNP) * Acute onset of symptoms of cardiac dysfunction: dyspnea, palpation, chest pain, and/or syncope; * Image for cardiac injury: marked diffused reduction in left ventricle wall movement, with dramatically decreased left ventricle ejection fraction (LVEF) \< 45%, or by cardiac magnetic resonance imaging.

Exclusion criteria

* Also considering acute coronary syndrome but unable to perform coronary angiography to distinguish acute coronary syndrome from myocarditis, or otherwise suffer from valvuloplasty. * Myocardial injury caused by sepsis, medical agents, or poisons; * Malignancy or any comorbidity limiting survival or conditions predicting inability to complete the study

Design outcomes

Primary

MeasureTime frameDescription
To assess heart failure questionnaire in patients that developed acute myocarditis3 yearsKCCQ will be fill at least once a year.
To assess CRP levels in patients that developed acute myocarditis3 yearsCRP levels in each clinical visit will be documented
To assess cardiac MRI in patients that developed acute myocarditis3 yearsCardiac MRI will be performed at least yearly and evaluated for regionally increased signal in T2-weighted images; Late gadolinium enhancement in a nonischemic pattern, Increased native T1 values on a 3T magnet.
To assess echocardiogram in patients that developed acute myocarditis3 yearsechocardiogram will be performed at least yearly and defined as normal, ST-segment elevation, with Diffuse or Non-diffuse changes, T-wave changes, Atrial fibrillation or non-sustained ventricular tachycardia.
To assess health quality by a questionnaire in patients that developed acute myocarditis3 yearsEQ-5D will be fill at least once a year. Descriptive analysis of EQ-5D profile at each observation and analysis of changes between repeated observations. Cluster analysis can be used.
To assess troponin levels in patients that developed acute myocarditis3 yearstroponin levels in each clinical visit will be documented
To assess PRO-BNP levels in patients that developed acute myocarditis3 yearsPRO-BNP levels in each clinical visit will be documented

Secondary

MeasureTime frameDescription
Chemokine in Patients after myocarditis3 yearsTo assess chemokines by measuring the serum concentrations
Hematopoietic Growth Factors (HGF)in patients after myocarditis3 yearsTo assess Hematopoietic Growth Factors in patients with COVID-19 by measuring the To assess HGF by measuring the serum concentrations
Complement in patients after myocarditis3 yearsassess complement factors by measuring the serum concentrations
Cytokine in Patients after myocarditis3 yearsTo assess cytokines by measuring the serum concentrations

Countries

Israel

Contacts

Primary ContactDror Mevorach, MD
mevorachd@hadassah.org.il972-2- 6777317

Outcome results

None listed

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