Assessing Coronary Non-Culprit Plaque Early with Start of PCSK9 Inhibitors in Acute Myocardial Infarction (ACCESS-AMI)
Condition(s) studied
Investigational drug(s) / intervention(s)
PCSK9 inhibitor: The patient used Trastuzumab 150mg within 24 hours before or after PCI, and then every two weeks for 12 months
Statin+ezetimibe: The patient used statins and ezetimibe within 24 hours before or after PCI, and then once a day for 12 months
Blood lipid levels meet the recommended guidelines: Early use of intensified lipid-lowering therapy during hospitalization led to a rapid decrease in blood lipids and met the recommended guidelines.
Blood lipid levels don't meet the recommended guidelines: The patient did not receive intensified lipid-lowering treatment during hospitalization or did not meet the recommended guidelines for blood lipids
Study summary
This study is planned to start on January 2024.
The goal of this clinical trial is to learn whether the perioperative administration (within 24 hours before or after primary PCI) of PCSK9 inhibitors can ameliorate plaque progression and adverse outcomes in patients with acute myocardial infarction (AMI). The main questions it aims to answer are:
Can perioperative PCSK9 inhibition improve the plaque stability and inflammation of perivascular adipose tissue (index of plaque attenuation(IPA )and perivascular fat attenuation index(FAI)) of non-target lesions? Researchers will compare PCSK9 inhibitors with statin plus ezetimibe therapy to evaluate the potential of PCSK9 inhibitors in mitigating the progression of non-target lesion plaques and reducing adverse cardiovascular events in patients with AMI.
Participants will:
Take PCSK9 inhibitors every two weeks or daily statin plus ezetimibe therapy. Conduct a follow-up examination with optical coherence tomography (OCT) or coronary computed tomography angiography (CTA) after 12 months.
Record the occurrence of major adverse cardiovascular events.
Eligibility
Primary outcome measure(s)
- Changes in Index of Plaque Attenuation (IPA) measured by OCT for non-culprit lesions at baseline and 12 months of follow-up. — 12 months
IPA is a quantitative analysis tool based on OCT technology to evaluate plaque stability. - Changes in pericoronary artery fat attenuation index (FAI) measured by CCTA for non-culprit lesions at baseline and 12 months of follow-up — 12 months
FAI is a quantitative indicator of inflammation in perivascular adipose tissue measured by CCTA.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Chinese PLA General Hospital | Beijing | Beijing Municipality | |
| Chinese PLA General Hospital [ | Beijing | China |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06854523 on ClinicalTrials.gov ↗ ← All trials in China