European Registry On Plaque ModifiCAtion in the STEMI Population (ROCA-STEMI)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Target Vessel Failure
研究概览
简要总结
This is an European prospective cohort study from February 2023 until February 2024. The investigators want to analyze the clinical success, efficacy and safety of consecutive patients who presented with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) for de novo heavily calcified culprit lesion using plaque modification devices before stent implantation.
详细描述
The ROCA-STEMI study is an European prospective cohort study from February 2023 until February 2024. The investigators want to analyze the clinical success, efficacy and safety of consecutive patients who presented with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) for de novo heavily calcified culprit lesion using plaque modification devices before stent implantation.
Clinical and angiographic endpoints will be defined according to the recommendations of the Academic Research Consortium. Academic Research Consortium represents a step toward standardization, facilitating the evaluation of the safety and effectiveness of devices.
Bleeding as a safety endpoint will be defined according to the Bleeding Academic Research Consortium. Major bleeding will be defined as Bleeding Academic Research Consortium types 3 and 5.
Severe coronary calcified lesion: Imaging evidence of severe calcium at the culprit lesion site was based on the angiographic presence of radio-opacities noted without cardiac motion before contrast injection involving both sides of the arterial wall in at least 1 location, or presence of ≥270° of calcium at 1 cross-section through IVUS.
Major adverse cardiovascular events (MACE): will be defined as the composite of cardiac death; MI; stroke, and revascularization, including percutaneous coronary intervention, and coronary artery bypass graft. Deaths will be regarded to be attributable to a cardiac cause unless a non-cardiac death could be confirmed.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years
- •Patient with a STEMI
- •Primary percutaneous coronary intervention
- •De-novo culprit lesion in a native coronary artery
- •Severe calcification of the target lesion or its equivalent (balloon uncrossable or undilatable lesion) (See Definitions 4.4)
- •Mandatory use of a plaque modification device to treat the culprit lesion (See Study device and procedures 4.5)
- •The patient or legal representative signing an informed written consent
排除标准
- •The target vessel had a stent from a previous PCI
- •The target lesion was treated as a staged procedure
- •Pregnant women
- •Terminally ill patients
结局指标
主要结局
Target Vessel Failure
时间窗: 12 months
The occurrence of cardiac death, target vessel myocardial infraction and target vessel revascularization.
次要结局
- Cardiac death(12 months)
- Major Adverse Cardiac Events (MACE)(12 months)
- Target vessel revascularization(12 months)
- Target lesion revascularization(12 months)
研究者
Héctor Cubero Gallego, MD, PhD
Principal Investigator
Hospital del Mar
