Cardiomyopathy Trial, Recruiting NCT05046002 Sponsor: Ottawa Heart Institute Research Corporation Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT05046002
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who were eligible to receive a COVID-19 vaccine.
  • People who experienced at least one heart-related symptom within 42 days of a COVID-19 vaccine, such as chest pain, chest pressure or discomfort, shortness of breath or pain when breathing, a pounding or irregular heartbeat, heavy sweating, fainting, or sudden cardiac arrest.
  • People who experienced at least two general (non-specific) symptoms within 42 days of a COVID-19 vaccine, such as fatigue, abdominal pain, dizziness or fainting, swelling, or cough.
  • People with no symptoms but who have abnormal tissue test results, or a combination of abnormal heart blood test results and abnormal heart scan results (ultrasound or MRI).
  • People who also have at least one of the following findings: elevated heart enzyme levels in blood tests (Troponin T, Troponin I, or CK-MB); an abnormal heart MRI; new or worsening irregular heart rhythms on a heart tracing or monitor; abnormal heart ultrasound findings; a specific sound or pulse finding detected during a physical exam; fluid around the heart or signs of inflammation seen on a scan, or elevated inflammation markers in blood tests; an enlarged heart seen on a chest X-ray; or evidence of heart muscle inflammation found during tissue examination (at autopsy or biopsy).

Who may not be able to join:

  • People whose symptoms and findings are clearly explained by another condition unrelated to the vaccine, such as Lyme disease affecting the heart or an autoimmune heart condition.
  • People whose symptoms began more than 42 days after receiving a COVID-19 vaccine.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Peter Liu, MD, Ottawa Heart Institute Research Corporation

Phone: 6136967351

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Ottawa Heart Institute Research Corporation
Registry
ClinicalTrials.gov
Start date
11 August 2021
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Proportion of patients with autoimmune disease; Composite of MACE

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov