Usual Dose Rosuvastatin Plus Ezetimibe Versus High-dose Rosuvastatin on Coronary Atherosclerotic Plaque

Phase 4

Active, not recruiting

• Conditions: Coronary Artery Disease
• Interventions: Drug: Rosuvastatin 20 mg orally once a day; Drug: Rosuvastatin 10 mg plus ezetimibe 10 mg orally once a day

• Registration Number: NCT03169985
• Lead Sponsor: Samsung Medical Center

Brief Summary

The aim of this prospective, open-label, randomized, single center study is to compare the effect of usual dose rosuvastatin plus ezetimibe and high-dose rosuvastatin on modifying atherosclerotic plaque.

Detailed Description

High-intensity statin therapy have shown improved clinical outcomes compared to placebo or moderate-intensity statin therapy. Based on these results, 2013 American College of Cardiology/American Heart Association(ACC/AHA) guideline on treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults recommended high-intensity statin therapy to patient with coronary artery disease for secondary prevention. However, high-intensity statin therapy was known to increase risk of diabetes mellitus and complication such as hepatotoxicity and myalgia. An alternative to high-intensity statin therapy is reducing the dose of statin and using drug that can improve blood cholesterol level by a different mechanism than statin. Ezetimibe acts on Niemann-Pick C1-like protein then inhibits cholesterol absorption in the intestine, which can reduce low-density lipoprotein(LDL) cholesterol more effectively when administered with statin. In IMPROVE-IT study, simvastatin plus ezetimibe decreased ischemic events more than simvastatin alone in patients with acute coronary syndrome. Although this study could confirm the additional effect of ezetimibe by using the same amount of simvastatin in both groups, it could not compare the effect of statin plus ezetimibe and high dose statin monotherapy. Moreover, there were few data on the efficacy of ezetimibe added to rosuvastatin which is one of the effective statin recommended by various guidelines. One study reported that rosuvastatin 2.5 mg plus ezetimibe 10 mg was superior to rosuvastatin 5 mg monotherapy in reducing LDL cholesterol. Another study reported that adding rosuvastatin 5 mg to ezetimibe 10 mg was more effective than rosuvastatin 5 mg alone in reducing coronary atherosclerotic lesions as measured by intravascular ultrasound. However, the previous studies did not compare the efficacy of combination therapy of usual dose rosuvastatin and ezetimibe to high-dose statin monotherapy. Therefore, investigators aimed to compare the effect of rosuvastatin 10 mg plus ezetimibe 10 mg to rosuvastatin 20 mg alone on the reduction of coronary atherosclerosis in patient with coronary artery disease. If this study shows that the combination of usual dose rosuvastatin and ezetimibe is not inferior to high dose rosuvastatin monotherapy in anti-atherosclerotic effect and safety, it would provide a basis for effective and safe cholesterol treatment.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2017-05-24
• Study First Submitted QC: 2017-05-26
• Study First Posted: 2017-05-30
• Study Start: 2017-07-12
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-19
• Last Update Posted: 2024-04-22
• Primary Completion: 2027-01-28
• Study Completion: 2027-01-28

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 280

Inclusion Criteria

• Among patients who undergo CAG for suspected ischemic heart disease and meet all of the followings:

  • Moderate stenosis (30-70%) in coronary artery
  • Deferred to medical treatment based on physiologic (FFR, CFR, IMR) or radiologic (IVUS with or without OCT) evaluation.

• Agreement obtained by participant

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Exclusion Criteria

• Severe renal failure(glomerular filtration rate < 30 ml/min/1.73m2, hemodialysis or peritoneal dialysis)

• Active liver disease

• Patient taking Niacin or fibrate(if possible, patient can be enrolled to the study after stopping those medication)

• Medical or family history of myositis, unexplained CK elevation > 3 times ULN at first visit

• Life expectancy < 2 years (judged by investigator)

• Coadministration of cyclosporine

• Untreated hypothyroidism

• Patient with poor compliance including alcohol abuse

• History of hypersensitivity including myotoxicity for either statin or ezetimibe

• Pregnant or breast-feeding woman

• Other conditions inappropriate for enrollment by investigator

  • * Eligible patients will be randomly assigned to treatment arms, stratified by diagnosis on admission(acute coronary syndrome or stable ischemic heart disease) and presence of chronic statin use (more than one month)

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
High-dose rosuvastatin monotherapy arm	Rosuvastatin 20 mg orally once a day	In patients who have moderate stenosis(30-70%) in coronary artery and deferred to medical treatment by intracoronary physiologic or radiologic test, this arm will be received rosuvastatin 20 mg qd during 12 months after randomization.
Rosuvastatin plus ezetimibe arm	Rosuvastatin 10 mg plus ezetimibe 10 mg orally once a day	In patients who have moderate stenosis(30-70%) in coronary artery and deferred to medical treatment by intracoronary physiologic or radiologic test, this arm will be received rosuvastatin 10 mg plus ezetimibe 10 mg qd during 12 months after randomization.

Primary Outcome Measures

Name	Time	Method
Change in percent atheroma volume(PAV) in non-culprit lesions	12 months after index coronary angiography(CAG)	PAV is calculated as the percentage of the sum of external elastic membrane(EEM) cross sectional areas(CSA) occupied by total atheroma volume(TAV). TAV was determined by summation of the plaque area, defined as the difference between EEM and lumen CSA, for all evaluable images. These values could be expressed as follows: TAV = ∑(EEM CSA - lumen CSA), PAV = 100 X ∑(EEM CSA - lumen CSA) / ∑EEM CSA

Secondary Outcome Measures

Name	Time	Method
Change in index of microcirculatory resistance(IMR)	12 months after index CAG	Physiologic index
Change in homeostatic model assessment(HOMA) index	6 months after index CAG	HOMA index is a method used to quantify insulin resistance. This values could be calculated with fasting plasma glucose and insulin, as follows: HOMA index = glucose X insulin (mg/dL) / 405
Change in fibrous cap thickness by OCT(optical coherence tomography)	12 months after index CAG	In case that OCT is conducted
Change in fractional flow reserve(FFR)	12 months after index CAG	Physiologic index
Change in normalized TAV in non-culprit lesions	12 months after index CAG	The TAV is normalized to the length corresponding to the median number of comparable slices for each treatment group in view of the variability in the length of pullback analyzed between subjects. This value could be expressed as follows: normalized TAV = \[∑(EEM CSA - lumen CSA) / number of images in pullback\] X median number of images in cohort
Change in indexed TAV	12 months after index CAG	Indexed TAV is calculated as TAV divided by the length of plaque in each subject. This value could be expressed as follows: Indexed TAV = ∑(EEM CSA - lumen CSA) / plaque length
Change in fasting glucose	6 and 12 months after index CAG	For risk of developing diabetes mellitus by statin therapy
Change in TAV in coronary computed tomography(CT) angiography	24 months after index CAG	TAV which is measured in CT angiography
Change in lipid profile	1, 6 and 12 months after index CAG	Fasting plasma triglyceride(TG), high-density lipoprotein(HDL), LDL and total cholesterol. These items will be compared separately, and described as a group of lipid profile.
Change in coronary flow reserve(CFR)	12 months after index CAG	Physiologic index
Major adverse cardiovascular events(MACE)	12, 24 and 36 months after index CAG	MACE is defined as a composite of death, myocardial infarction, stroke and revascularization.
Change in hemoglobin A1c	6 and 12 months after index CAG	For risk of developing diabetes mellitus by statin therapy
Change in high-sensitivity C-reactive protein(hs-CRP)	1 and 12 months after index CAG	hs-CRP
Safety endpoint: Number of participants with abnormal laboratory values and adverse events	1 and 12 months after index CAG	1. Creatine kinase(CK) elevation \> 10 times upper limit of normal(ULN); 2. CK elevation \> 10 times ULN on two consecutive visits; 3. Hepatic transaminases \> 3 times ULN; 4. Hepatic transaminases \> 3 times ULN on two consecutive visits; 5. Document reason for discontinuation of study medication; These items will be described together as a group of safety endpoint, such as number of participants with abnormal laboratory values and adverse events.

Trial Locations

Locations (1)

Samsung Medical Center; 🇰🇷 Seoul, Korea, Republic of