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Study identifier: NCT04731155 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingPERFECT-AMI

Impact of Early PCSK9 Inhibitor on Heart After Acute Myocardium Infarction

Condition: Early PCSK9 Inhibitor on Ventricular Remodling  ·  Sponsor: Shanghai Tong Ren Hospital

PhasePhase 4
Planned participants20
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where2 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This is a prospect, multi-center, random study to investigate whether early offering PCSK9 inhibitor to acute myocardium infarction(AMI) can alleviate ventricular remodeling after primary percutaneous intervention(PPCI). Totally,twenty acute myocardium infarction subjects will be enrolled in this study after consent information. After randomization, the control group will receive standard therapy for AMI including PPCI. The experiment group will receive first PCSK9 inhibitor before PPCI, then twice a month until 3 months later. Six month after AMI, Myocardial salvage index will be used to evaluate ventricular remodeling. TnI peaking time and LDL control rates also will be recorded and compared.

This description comes directly from the study's public registry record.

Talk to the study team

Lei Hou, Doctor  ·  13564868096  ·  Dr_houlei@163.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Subject must be at least 18 years of age and less than 80 years old 2. Patients should have undergone successful percutaneous coronary intervention with drug-eluting stent for AMI and LAD should be the only culprit vessel. 3. Subject understand the study requirements and the treatment procedures and provided informed consent before the procedure Exclusion Criteria: 1. Female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study 2. Known hypersensitivity or contraindication to study medications 3. Plan to receive revascularization in next six month. 4. Have received revascularization before. 5. Subjects with life expectation less than one year. 6. Subjects with active malignant tumor 7. subjects with severe liver or renal dysfunction(ALT \>5倍ULA,eGFR\<15ml/min/1.73mm2) 8. Other conditions which the investigators think not applicable to the study.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (2)

Tongren Hospital, ShanghaiShanghai, Shanghai Municipality, ChinaRecruiting
Shanghai tenth people's hospitalShanghai, ChinaRecruiting

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Shanghai

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