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MRNA COVID-19 疫苗接种后心肌炎和/或心包炎国家监测研究 (MYCOVACC)

2026年11月2日 更新者:Cardiology Research UBC

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.

研究概览

研究类型

观察性的

注册 (估计的)

500

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • British Columbia
      • Vancouver、British Columbia、加拿大、V5Z 1M9
        • 招聘中
        • Vancouver General Hospital
        • 接触:
        • 首席研究员:
          • Nathaniel Hawkins, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

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"

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:COHORT
  • 时间观点:PROSPECTIVE

队列和干预

团体/队列
干预/治疗
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

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
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)
大体时间:From date of vaccination and up to 3 years

Including 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.
From date of vaccination and up to 3 years
Recovery of cardiac function in patients with previously documented abnormal cardiac function
大体时间: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
大体时间: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
大体时间: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
大体时间:Through study completion, an average of 3 years

Physical activity: International Activity Questionnaire.

Through study completion, an average of 3 years

次要结果测量

结果测量
大体时间
MRNA COVID-19 疫苗接种后 30 天和 42 天的主要复合终点的各个组成部分?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年
MRNA COVID-19 疫苗接种后房性心律失常的发生率?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年
MRNA COVID-19 疫苗接种后全因死亡率和心血管死亡率的发生率?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年
MRNA COVID-19 疫苗接种后全因和心血管住院率?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年
接种 mRNA COVID-19 疫苗后心肌炎/心包炎的复发率?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年
接种 mRNA COVID-19 疫苗后缩窄性心包炎的发生率?
大体时间:自接种疫苗之日起最长三年
自接种疫苗之日起最长三年

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Nathaniel Hawkins, MD、Vancouver General Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

有用的网址

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2023年4月23日

初级完成 (估计的)

2027年3月23日

研究完成 (估计的)

2027年4月23日

研究注册日期

首次提交

2023年5月29日

首先提交符合 QC 标准的

2023年10月24日

首次发布 (实际的)

2023年10月26日

研究记录更新

最后更新发布 (实际的)

2026年11月3日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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