The Prognostic Value of Cardiopulmonary Exercise Testing Parameters in Patients With Coronary Heart Disease: A Retrospective Cohort Study(CPETPCAD)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorXinjiang Medical University

About this trial

Parameters related to cardiopulmonary exercise testing (CPET) are important objective indicators for evaluating cardiopulmonary function in patients with coronary heart disease. However, the clinical application of CPET parameters in the prognostic assessment of patients with coronary heart disease remains unclear. This is a retrospective cohort study designed to systematically collect real-world clinical data and long-term follow-up outcomes of patients with coronary heart disease. Through standardized follow-up, this study will investigate the association between CPET parameters and adverse clinical outcomes in patients with coronary heart disease, as well as the relevant risk factors.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Our hospital has diagnosed coronary heart disease and conducted cardiopulmonary exercise tests.

Patients with complete clinical data.

Disqualifiers

Uncontrolled heart failure (NYHA classification Ⅲ-IV grade).

Complications, such as moderate to severe anemia, tumors and lung diseases.

Complicated with valvular heart disease.

Unable to reach the anaerobic threshold during exercise.

Trial population

Patients diagnosed with coronary heart disease in our hospital and who have completed cardiopulmonary exercise testing.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

15,000 Participants
are grouped into 1 trial group
Group A: Coronary Heart Disease Cohort

Trial outcomes

Primary outcomes

1

Cumulative incidence of Major Adverse Cardiovascular Events (MACE)

The proportion of patients who experience an adjudicated Major Adverse Cardiovascular Event (MACE), defined as a composite endpoint consisting of non-fatal myocardial infarction, non-fata

Time frame
1 year

Secondary outcomes

1

All-cause mortality

Record of deaths from any cause during follow-up. Confirmed by medical records, family follow-up, or national death registration systems.

Time frame
1 year

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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