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Recruiting NCT06567418

NCT06567418 Retrospective Analysis of the Effect of In-hospital Initiation of PCSK9i on Clinical Outcomes in Chinese ACS Patients

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Clinical Trial Summary
NCT ID NCT06567418
Status Recruiting
Phase
Sponsor Yun Dai Chen
Condition Acute Coronary Syndrome
Study Type OBSERVATIONAL
Enrollment 10,000 participants
Start Date 2024-08-01
Primary Completion 2024-08-31

Trial Parameters

Condition Acute Coronary Syndrome
Sponsor Yun Dai Chen
Study Type OBSERVATIONAL
Phase N/A
Enrollment 10,000
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-08-01
Completion 2024-08-31
Interventions
alirocumab 75mg/2weekstatin ± ezetimibe

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Brief Summary

The objective of this study is to investigate the effectiveness of in-hospital initiation of alirocumab combined with statin ± ezetimibe on major cardiovascular events (MACE) in Chinese ACS patients. The main question it aims to answer is: whether early initiation PCKS9i in hospital could reduce recent cardiovascular event risk in Chinese ACS patients in real-world setting. Data from CCA Database-Chest Pain Center were screened for all ACS patients from 01-Jan 2021 to 31-Dec 2023. Patients diagnosed with STEMI, NSTEMI or UA at admission were identified at the first step. Then, for intervention group, patients who received alirocumab 75mg combined with statin ± ezetimibe during the ACS hospitalization (including the discharge date) will be included; for control group, patients who received statin ± ezetimibe during the ACS hospitalization will be included. All enrolled patients were required to have at least one documented follow-up visit.

Eligibility Criteria

Inclusion Criteria: * Patients diagnosed with Acute Coronary Syndrome (ACS) upon hospital admission. * Patients aged 18 years or older. * Patients who received Alirocumab 75 mg in combination with statin therapy ± Ezetimibe as the intervention group, and those treated exclusively with statin therapy ± Ezetimibe as the control group, either during hospitalization or at discharge. * Patients with at least one follow-up record. Exclusion Criteria: * Patients who received Evolocumab treatment at any time. * Patients who received Inclisiran treatment at any time.

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