Intensive Cholesterol-Lowering Within 24 Hours of PCI Perioperative Period

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital of Nanchang University

About this trial

This project team is conducting a multicenter randomized controlled study, aiming to administer PCSK9 inhibitors subcutaneously as early as possible within 24 hours during the perioperative period of AMI (included \<24h STEMI and NSTEMI), and subsequently once every 12 weeks for a total of 6 months, followed by step-down therapy according to guideline-recommended lipid-lowering strategies based on LDL-C target levels. The study will evaluate changes in blood lipids and inflammatory markers during hospitalization and at follow-up visits at 1, 3, 6, 9, and 12 months, as well as the incidence of MACE events. Safety will also be assessed, including liver enzymes, kidney function, and other adverse reactions. Compared with conventional treatment, the study will test efficacy and ultimately clarify that early combined use of PCSK9 inhibitors during the perioperative period of AMI patients can safely and effectively reduce LDL-C, control systemic inflammatory responses, and improve the incidence of MACE events.

Eligibility criteria

Qualifiers

Age ≥18 years;

Meet the definition of acute myocardial infarction according to the "2019 Guidelines for the Diagnosis and Treatment of Acute ST-Segment Elevation Myocardial Infarction", including STEMI and NSTEMI with onset <24 hours;

Able to understand and voluntarily sign the informed consent form.

Disqualifiers

Severe mental disorders that prevent the expression of consent;

Severe heart failure (Killip class III or IV) or cardiogenic shock;

According to the investigator's judgment, the presence of significant other abnormal signs, laboratory findings, or clinical conditions (such as tumors, shock, liver or kidney failure, etc.) that make participation unsuitable;

Investigator's judgment that the subject cannot complete long-term follow-up;

Trial design

Treatments tested in this trial

  • Recaticimab

Treatment groups

2,442 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Second Affiliated Hospital of Nanchang University

Lead sponsor

First Affiliated Hospital of Gannan Medical University

Collaborator

Jiujiang No.1 People's Hospital

Collaborator

First People's Hospital of FuZhou

Collaborator

Yueyang Central Hospital

Collaborator

The First People's Hospital of Changde City

Collaborator

ZhuZhou Central Hospital

Collaborator

Xiangtan Central Hospital

Collaborator

Loudi Central Hospital

Collaborator