Recruiting
Observational
Efficacy and Safety of Comprehensive Treatment in Patients With IR-CAD: a Self-controlled Cohort Study
Condition(s) studied
Coronary Artery DiseaseCoronary Artery StenosisCoronary Artery RestenosisCoronary Artery Disease ProgressionInflammationInflammatory DiseaseInflammation Vascular
Investigational drug(s) / intervention(s)
Healthy life styleSecondary prevention for atherosclerotic coronary artery diseaseImmunosuppressive therapyCoronary revascularizationSupportive therapies
Healthy life style: Healthy diet, regular exercise, and quitting smoking
Secondary prevention for atherosclerotic coronary artery disease: Antiplatelet therapy, as well as medications for control of heart rate, blood pressure, low-density lipoprotein cholesterol, and blood glucose
Immunosuppressive therapy: Glucocorticoids and/or immunosuppressive agents
Coronary revascularization: Percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG).
Supportive therapies: Medical interventions for prevention and treatment of the side effects of the above treatment, such as abnormal liver function, hypocalcemia, hypokalemia, peptic ulcer, infection, et al.
Study summary
This is a self-controlled cohort study to evaluate the efficacy and safety of comprehensive treatment in patients with inflammation-associated rapidly-progressive coronary artery disease (IR-CAD) by comparing the study endpoints before treatment with those after treatment in the same group of patients.
Eligibility
Inclusion Criteria:
1. Fulfilling all the following criteria before initiation of comprehensive treatment:
1.1 18 years of age or older, male or female.
1.2 Negative result of urine or blood pregnancy test for females with childbearing potential (not post-menopausal or surgically sterile).
1.3 Prior history of coronary revascularization (percutaneous coronary intervention \[PCI\] or coronary artery bypass graft \[CABG\]).
1.4 Receiving standard treatment for secondary prevention of atherosclerotic coronary artery disease (AS-CAD) after the last coronary revascularization.
1.5 Hospitalization due to rapidly-progressive myocardial ischemia:
* Typical symptoms of angina (Canadian Cardiovascular Society \[CCS\] III-IV) and non-invasive evidence of myocardial ischemia; and
* Occurred within 6 months or occurred on immunosuppressive therapy within 12 months of the last coronary revascularization.
1.6 Angiographic evidence of new coronary lesions (de novo stenoses or restenoses):
* Occurred after the last coronary revascularization; and
* Related to myocardial ischemia (location, extent, severity, et al).
1.7 Evidence of inflammation:
* At least one of the markers indicating active inflammation has ever been elevated (erythrocyte sedimentation rate \[ESR\], high-sensitivity C-reactive protein \[hs-CRP\], interleukin \[IL\]-6, tumor necrosis factor \[TNF\]-α, ferritin, et al); or
* Established diagnosis of systemic autoimmune disease or systemic vasculitis; or
* Receiving immunosuppressive therapy.
2. Receiving comprehensive treatment, including ischemia-driven PCI which was performed no earlier than 40 days of the initiation of immunosuppressive therapy.
Exclusion Criteria:
1. Coronary restenosis due to mechanical factors (stent under-expansion, stent mal-apposition, stent rupture, et al).
2. Other moderate to severe heart diseases (congenital heart disease, valvular heart disease, myocarditis, cardiomyopathy, pericardial diseases, pulmonary hypertension, heart failure, arrhythmia, et al).
3. Active acute or chronic infection (human immunodeficiency virus \[HIV\], tuberculosis, et al).
4. Active malignancy (diagnosed within 12 months or with ongoing requirement for treatment).
5. Vital organ failure.
6. Life expectancy \< 1 year.
7. Contraindications for or intolerance to treatment for secondary prevention of AS-CAD, contrast agents, glucocorticoids, immunosuppressive agents.
8. In pregnancy or breast-feeding, or with intention to be pregnant during the study period.
9. Risk of non-compliance (history of drug addiction or alcohol abuse, et al).
10. Previous enrollment in this study.
11. Participation in another study within 30 days.
12. Involvement in the planning and conduct of this study (applying to investigators, contract research organization staffs, study site staffs, et al).
13. Any condition, which in the opinion of the investigators, would make it unsuitable for the patient to participate in this study.
Primary outcome measure(s)
- Major adverse cardiovascular events (MACE) — Time from the last coronary revascularization to the first occurrence of MACE, or the last follow-up visit, or the end of 24-month follow-up, which occurs first, both before and after the initiation of comprehensive treatment.
The composite endpoint including death, or Q wave myocardial infarction, or unplanned myocardial ischemia-driven coronary revascularization (PCI or CABG), or unplanned myocardial ischemia-driven hospitalization.
Trial sites (1)
| Facility | City | Region | Status |
| Peking Union Medical College Hospital |
Beijing |
Beijing Municipality |
Recruiting |
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