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A prospective multiCenter randomized contrOlled study of intracavitary multimodal imaging evaluating the clinical outcomeS of intensive lipid-regulation Therapy in patients with acute coronary syndrome

A prospective multiCenter randomized contrOlled study of intracavitary multimodal imaging evaluating the clinical outcomeS of intensive lipid-regulation Therapy in patients with acute coronary syndrome - cost study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076092
Enrollment
Unknown
Registered
2023-09-25
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-10-03

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

Conditions

acute coronary syndrome

Interventions

Control group :? Control group (standard treatment group, n=268) : meeting the inclusion criteria and successfully completing infarct-related PCI, receiving placebo, subcutaneous injection, atorvastat
Intensive group:? Intensive group (standard treatment + Aliciumab, n=268) : those who met the inclusion criteria and successfully completed infarct-related PCI were given subcutaneous injection of ali

Sponsors

the second hospital of tian jin medical university tian jin china
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: ? Over 18 years old, less than 85 years ? ACS patients who successfully underwent PCI for infarction (STEMI, NSTEMI) ? Non-blocking lesions in non-infarcted vessels (50%-70% stenosis) ? Patients who received regular statin treatment 4 weeks before inclusion but LDL-C=70mg/dl ? Patients with LDL-C=125mg/dl who did not receive regular statin treatment 4 weeks before inclusion

Exclusion criteria

Exclusion criteria: (1) Pregnant women (2) Implanted stent diameter 4.0mm (3) need to stop with the current medical condition within 24 months after enrollment, life expectancy 1.5xULN); (14) Active peptic ulcer; (15) Oral anticoagulants are also required; (16) Platelets below 100x 10 ?/L; (17) Hemoglobin below 90g/L; (18) Pregnancy or lactation; (19) Patients participating in other interventional clinical studies; (20) The researchers believe that patients who are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
all cause death;ogenic death; nonfatal myocardial infarcti;ichemic event-driven coronary revascularization;

Secondary

MeasureTime frame
percentage of atherosclerotic plaque volume in non-infarcted vessels (PAV), ;minimum fiber cap thickness in non-infarcted vessels ;

Countries

China

Contacts

Public ContactXU YANMIN

the second hospital of tian jin medical university tian jin china

xuyanminphdmd@163.com+86 137 0202 9695

Outcome results

None listed

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