Coronary Artery Disease Clinical Trial
Official title:
Evaluation of the Strategy of "One-stop" Endovascular Treatment for Concomitant Coronary Artery Disease and Aortic Atherosclerotic Disease
The study is designed to evaluate the safety and effectiveness of the "one-stop" endovascular intervention strategy for patients with concomitant coronary artery disease and aortic atherosclerotic disease. It is a registration study, which will consecutively enroll at least 50 patients with at least 30 subjects receiving one-stop strategy.
Status | Not yet recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Aged from 18 years to 75years, male or female; - Aortic atherosclerotic disease with the indication of EVAR; - Coronary heart disease with the indication of PCI; - Provided informed consent. Exclusion Criteria: - Acute aortic dissection - Acute coronary syndrome - Dysfunction of coagulation system - Patients with gastrointestinal hemorrhage - Known allergy to contrasts or antiplatelet drugs - Renal dysfunction (GFR=60ml/min) - Patient with multi-branch coronary preferred CABG |
Country | Name | City | State |
---|---|---|---|
China | Chinese Academy of Medical Sciences, Fuwai Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Chinese Academy of Medical Sciences, Fuwai Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Treatment-Emergent Adverse Events | The incidence of a composite endpoint of all-cause mortality, myocardial infarction, rupture of aorta, hematoma, bleeding events (BARC=2 grade), pseudoaneurysm, stent thrombosis | 12 months | |
Secondary | Operative success rate | 12 months | ||
Secondary | Average in-patient time | 12 months | ||
Secondary | Average cost during hospitalization | 12 months |
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