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Early initiation of intensification lipid lower treatment in hospitalized ACS patients: a prospective, multi-center, observational study

Early initiation of intensification lipid lower treatment in hospitalized ACS patients: a prospective, multi-center, observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065861
Enrollment
Unknown
Registered
2022-11-17
Start date
2022-11-17
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

coronary artery disease

Interventions

Statin monotherapy Group:N/A
Statin + Ezetimibe Group:N/A
Statin + Aliciumab Group:N/A

Sponsors

Chinese PLA Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Recent (within 52 weeks of alirocumab treatment Index Initiation) ACS requiring hospitalization. The ACS can be ST-elevation MI (STEMI), non-ST elevation MI (NSTEMI) or high-risk unstable angina (UA), and is defined by ischemic symptoms with unstable pattern, occurring at rest or minimal exertion within 72 hours of an unscheduled hospital admission, due to proven obstructive coronary disease and at least one of the following: (1) Elevated cardiac biomarkers; (2) Resting electrocardiogram (ECG) changes consistent with ischemia or infarction; (3) LDL-C >= 70 mg/dL (>= 1.8 mmol/L) assessed prior to patients who have been receiving any stable statin regimen within >= 4 wk prior to enrolment; OR LDL-C >= 100 mg/dL (>= 2.6 mmol/L) in patients who are statin-naive or have not been on stable statin regimen for >= 4 wk prior to enrollment; (4) Written informed consent obtained from eligible patients prior to registration enrollment in the study.

Exclusion criteria

Exclusion criteria: 1. PCSK9 inhibitors were administered within 3 months before Index Initiation; 2. Patient with any severe life-threatening conditions, including severe hepatic impairment, severe renal failure; 3. Patient with history of renal transplantation, heart transplantation; 4. Patient is a pregnant or lactating woman, or woman intending to become pregnant; 5. Other conditions unsuitable assessed by the investigators.

Design outcomes

Primary

MeasureTime frame
Basic vital signs;routine blood test;Blood biochemistry;Inflammatory factor;urinalysis;myocardial damage markers;12-lead ECG;Coronary computed tomography angiography;

Countries

China

Contacts

Public ContactYundai Chen

Cardiology Department of Chinese PLA Hospital

cyundai@vip.163.com+86 13311119778

Outcome results

None listed

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