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Impact of dual lipid-lowing strategy of atorvastatin with ezetimibe on inflammatory mediators in patients with acute coronary syndrome undergoing elective percutaneous coronary intervention: a 2×2 factorial randomized controlled trial

Impact of dual lipid-lowing strategy of atorvastatin with ezetimibe on inflammatory mediators in patients with acute coronary syndrome undergoing elective percutaneous coronary intervention: a 2×2 factorial randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026762
Enrollment
Unknown
Registered
2019-10-21
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NSTE-ACS

Interventions

A20:atorvastatin 20mg/d
A20+E10:atorvastatin 20mg/d combined with ezetimibe10mg/d
A40:atorvastatin 40mg/d
A40+E10:atorvastatin 40mg/d combined with ezetimibe 10mg/d

Sponsors

The First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All the subjects in the study were in patients aged >= 18 years in the Department of Cardiology, First Hospital Affiliated with China Medical University (Shen yang, China) from March 2018 to June 2019.

Exclusion criteria

Exclusion criteria: 1. had a history of previous statin or ezetimibe therapy; 2. had a history of statin-induced myopathy or serious hypersensitivity reaction to statins and /or a history of hypersensitivity to any ezetimibe components; 3. had severe congestive cardiac failure (New York Heart Association class IIIb or IV); 4. had current active liver disease (alanine aminotransferase > 2 times the upper limit of normal [ULN]) or severe hepatic impairment, uncontrolled hypothyroidism, unexplained creatine kinase >1 ULN before enrollment or serum creatinine >176 mmol/l (2.0 mg/dl). 5. Women who were pregnant, breastfeeding, or of childbearing potential but not using contraception were also excluded, or other comorbidities, including infection, systemic immune diseases, pericarditis and malicious tumour.

Design outcomes

Primary

MeasureTime frame
lipoprotein-associated phospholipase A2;VCAM;

Secondary

MeasureTime frame
periprocedural myocardial injury;Major adverse cardiovascular events;statin-related myopathy;liver enzyme elevation;

Countries

China

Contacts

Public ContactDalin Jia

The First Affiliated Hospital of China Medical University

liang121682@163.com+86 13998802270

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026