Coronary Heart Disease
Conditions
Keywords
Coronary heart disease, Atherosclerosis, Acute myocardial infarction, Coronary intervention
Brief summary
In this study, simvastatin combined with Ezeimebum was used to enhance lipid reduction, and IVUS was used to evaluate the volume and composition of coronary plaque before and after treatment. The aim is to evaluate the overall intervention effect of Ezeimebum on stable angina pectoris with diabetes mellitus on the basis of statins.
Detailed description
This study was conducted in patients with stable angina pectoris complicated with diabetes mellitus in Chinese PLA General Hospital and coronary arteriography confirmed as critical lesion of coronary artery. The patients were randomly divided into two groups: ezeimebum combined with simvastatin group and simvastatin group. The patients of the former group were given ezeimebum 10mg combined with simvastatin 40mg for 12 months while the patients of the latter group were given simvastatin 40mg for 12 months. Assessed coronary atherosclerotic plaque volume percentage (PAV) and standardized total atherosclerotic plaque volume (TAV) by intravascular ultrasound (IVUS) at the time of entry and out of the group after 12 months. The changes of PAV level in both groups were taken as the main endpoints, and the changes of TAV levels in the two groups as the secondary endpoints. The changes of serum lipids and hypersensitive C-reactive protein levels were compared between the two groups before and after the treatment. Major cardiovascular events (non-fatal myocardial infarction, all-cause death, readmission to acute heart failure, and revascularization of recurrent angina pectoris) were followed up for 12 months.
Interventions
ezetimibe 10mg with simvastatin 40mg everyday for 12 months after PCI
DRUGSimvastatin
simvastatin 40mg everyday for 12 months after PCI
Sponsors
Chinese PLA General Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* patients aged 18-75 years * consistent with the Chinese criteria for the diagnosis of chronic stable angina pectoris, stable angina pectoris symptoms in the last three months, and no more than CCS grade 3 of angina pectoris * coronary angiography showed that the degree of coronary artery stenosis was 50% and 70% * LDL-C standard: LDL-C \> 80 mg/dL (2.08 mmol/L) * The patients diagnosed with type 2 diabetes were currently using hypoglycemic drugs or insulin * Sign the informed consent to join the group.
Exclusion criteria
* Acute coronary syndromes such as myocardial infarction, unstable angina pectoris, variant angina pectoris, cardiac shock, chronic heart failure, malignant arrhythmia, etc. * Patients requiring stent implantation had been treated with intensive statins prior to admission (e.g. doses of Atto vastatin 40mg or resuvastatin 20mg) * There were contraindications or statins for statin lowering lipids or statins, and there was a history of adverse reactions (liver injury, rash, myolysis, etc.) in the use of Ezeimebum, etc. * Severe liver and kidney dysfunction, creatinine clearance \< 30ml / min, acute pancreatitis, malignant tumor, etc.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from Baseline coronary plaque volume percentage(PAV) at 12 months | 12 months after PCI | PAV=∑（(ESA CSA-lumen CSA)/(ESA CSA)）x100, EEM CSA：cross-sectional area of outer elastic membrane boundary; lumen CSA: cross-sectional area of tube boundary |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| LDL-C | follow up in one year | Low density lipoprotein cholesterol (LDL-C) |
| HDL-C | follow up in one year | High density lipoprotein cholesterol (HDL-C) |
| Change from Baseline standardized coronary plaque volume(TAV) at 12 months | 12 months after PCI | TAV= (median number of images in ∑ (ESA CSA-lumen CSA) / retracement) x number of images (standardized according to the length of IVUS retracement, To ensure that each individual patient has the same weight) |
| TC | follow up in one year | Total cholesterol (TC) |
| Inflammation marker | follow up in one year | hs-CRP |
| TG | follow up in one year | Total triglyceride(TG) |
Countries
China
Contacts
Primary ContactGeng Qian, MD
Outcome results
None listed