COVID-19 Microvascular Evaluation Trial

Summary

The COMET trial is an observational, cross-sectional study aimed at comparing the incidence of coronary microvascular dysfunction (CMD) in patients with stable angina who have a history of severe COVID-19 infection requiring mechanical ventilation (Group A) to those without a history of COVID-19 (Group B). A total of 102 participants will be recruited, with 51 patients in each group. Data will be collected on participants' demographic information, medical history, and COVID-19 infection history (confirmed by PCR test). CMD measurement will be performed using a pressure-temperature wire to assess the coronary flow reserve and index of microcirculatory resistance. In addition, information on participants' current medications will be gathered. The study will employ statistical analysis tools to compare CMD incidence between the two groups and assess the impact of various factors such as age and sex on CMD incidence. The results of the COMET trial will provide valuable insights into the effects of severe COVID-19 infection on CMD in patients with stable angina.

Eligibility

Here's a detailed outline of the eligibility criteria, including inclusion, exclusion, and withdrawal criteria for the COMET trial. Please review and let me know if you need any further clarification or have additional information to provide.

Inclusion Criteria:

1. Patients with a clinical diagnosis of stable angina, consulted by a cardiovascular consultant and referred to undergo diagnostic coronary angiography.
2. Patients who are able to provide informed consent.
3. For Group A: Patients with a history of severe COVID-19 infection requiring mechanical ventilation, confirmed by a PCR test.
4. For Group B: Patients without a history of COVID-19 infection.

Exclusion Criteria:

1. Patients with unstable angina or acute coronary syndrome.
2. Patients with a history of myocardial infarction, percutaneous coronary intervention, or coronary artery bypass graft surgery.
3. Patients with known structural heart disease or valvular heart disease.
4. Patients who are unable to undergo intracoronary pressure-temperature wire measurement of CMD due to contraindications or other medical reasons.

Withdrawal Criteria:

1. Withdrawal of informed consent by the participant at any time during the study.
2. Development of an unstable medical condition or complication that prevents the participant from completing the study or makes it unsafe for them to continue.
3. Identification of exclusion criteria after enrollment that should have precluded the participant's inclusion in the study.
4. Non-compliance with study procedures or protocol deviations that may affect the validity of the study results.

Conditions3

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