跳至主要内容
临床试验/NCT04968808
NCT04968808
招募中
不适用

OPtimal TIming of Fractional Flow Reserve-Guided Complete RevascularizatiON in Non-ST-Segment Elevation Myocardial Infarction (OPTION-NSTEMI)

Chonnam National University Hospital2 个研究点 分布在 2 个国家目标入组 1,014 人2021年9月1日

概览

阶段
不适用
干预措施
Staged in-hospital complete revascularization
疾病 / 适应症
Myocardial Infarction, Acute
发起方
Chonnam National University Hospital
入组人数
1014
试验地点
2
主要终点
Cumulative incidence rate of all-cause death, non-fatal myocardial infarction, or all unplanned revascularization
状态
招募中
最后更新
5天前

概览

简要总结

Many patients with non-ST-segment elevation myocardial infarction (NSTEMI) have multivessel coronary artery disease (MVD), which is associated with poor clinical outcomes. However, there have been few studies regarding revascularization strategy in patients with NSTEMI and MVD. Therefore, we planned to perform prospective, open-label, randomized trial to evaluate the efficacy and safety of immediate complete revascularization (percutaneous coronary intervention [PCI] for both infarct-related artery [IRA] and non-IRA during index PCI) compared to staged PCI strategy of non-IRA (PCI for IRA followed by non-IRA PCI after several days). PCI procedure at non-IRA with diameter stenosis between 50 and 69% should be conducted with the aid of fractional flow reserve (FFR), and non-IRA with diameter stenosis ≥ 70% will be revascularized without FFR.

详细描述

Many patients with non-ST-segment elevation myocardial infarction (NSTEMI) have multivessel coronary artery disease (MVD), which is associated with poor clinical outcomes. In cases of hemodynamically stable ST-segment elevation myocardial infarction (STEMI) and MVD, many studies demonstrated the superiority of complete revascularization (CR) by both one-stage and multistage procedures compared to culprit-only revascularization (COR). The 2017 European Society of Cardiology (ESC) guidelines for STEMI recommend routine revascularization for non infarct-related artery (IRA) lesions before hospital discharge in patients without cardiogenic shock. However, there have been few studies regarding revascularization strategy in patients with NSTEMI and MVD. Only one randomized controlled trial, the SMILE trial (J Am Coll Cardiol 2016;67:264-72), compared one-stage and multi-stage multivessel revascularization (MVR) in these patients. Although the results of most studies analyzing interventional strategies in patients with NSTEMI and MVD showed superior results of MVR compared to COR, they did not provide information about staged revascularization. One-stage MVR was associated with better clinical outcomes compared to multi-stage MVR in the SMILE trial, while one-stage and multi-stage MVR had similar incidences of adverse outcomes in large registry data. Although the 2018 ESC/European Association for Cardio-Thoracic Surgery (EACTS) guidelines for myocardial revascularization recommend complete one-stage revascularization in NSTEMI and MVD, it emphasizes individualization based on clinical status and comorbidities, as well as disease severity. In 2020 ESC guidelines for non-ST-segment elevation acute coronary syndrome, this strategy is maintained. CR during index percutaneous coronary intervention (PCI) is recommended in NSTEMI patients with MVD (class IIb, level B). Whether to revascularize non-IRA using angiography or fractional flow reserve (FFR) is also problematic. FFR is a useful tool for assessing hemodynamic significance of non-IRA during both acute and subacute stage, and FFR-guided PCI for non-IRA lesion is recommended during index PCI (class IIb, level B). In the SMILE trial, a 25.8% of study patients received FFR-guided PCI for non-IRA. Although FFR is a well-known tool to evaluate significant ischemia of moderate stenosis, the most studies regarding FFR enrolled patients without acute myocardial infarction (AMI). However, the recommendations in current guidelines, which recommends CR during index PCI, is not sufficiently powered to assess differences in clinical outcomes between interventional strategy. There are also few studies regarding this issue, and discrepancy in clinical outcomes between randomized trial and observational studies. Furthermore, FFR-guided PCI for non-IRA is not mandatory in these studies. Therefore, we planned to perform prospective, open-label, randomized trial to evaluate the efficacy and safety of immediate complete revascularization (PCI for both IRA and non-IRA during index PCI) compared to staged PCI strategy of non-IRA (PCI for IRA followed by non-IRA PCI after several days). PCI procedure at non-IRA with diameter stenosis between 50 and 69% should be conducted with the aid of FFR, and non-IRA with diameter stenosis ≥ 70% will be revascularized without FFR.

注册库
clinicaltrials.gov
开始日期
2021年9月1日
结束日期
2028年8月31日
最后更新
5天前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Min Chul Kim

Associate Professor

Chonnam National University Hospital

入排标准

入选标准

  • Age ≥ 19 years old
  • Non-ST-segment elevation myocardial infarction
  • Angina pectoris or equivalent ischemic chest discomfort with at least 1 of 3 features and,
  • occurs at rest, usually lasting \> 10 minutes
  • severe and new onset (within the prior 4-6 weeks)
  • crescendo pattern
  • Elevated cardiac biomarkers and,
  • ≥ 99% value of high-sensitivity cardiac troponin
  • No ST-segment elevation ≥ 0.1 mV in ≥ 2 contiguous leads or newly developed left bundle branch block on 12-lead electrocardiogram
  • PCI within 72 hours after symptom development

排除标准

  • Cardiogenic shock at initial presentation or after treatment of IRA
  • TIMI flow at non-IRA ≤ 2
  • Severe procedural complications (e.g. persistent no-reflow phenomenon, coronary artery perforation) which restricts study enrollment by operators' decision
  • Non-IRA lesion not suitable for PCI treatment by operators' decision
  • Chronic total occlusion at non-IRA
  • History of anaphylaxis to contrast agent
  • Pregnancy and lactation
  • Life expectancy \< 1-year
  • Severe valvular disease
  • History of CABG, or planned CABG

研究组 & 干预措施

Staged in-hospital CR (complete revascularization)

Non-infarct related artery (IRA) will be revascularized in other day (during hospitalization) after percutaneous coronary intervention (PCI) for IRA. Non-IRA lesion which have equal or more than 70% diameter stenosis by visual estimation will be revascularized without fractional flow reserve (FFR) evaluation. Non-IRA lesion with diameter stenosis 50-69% by visual estimation will be evaluated using FFR device. In case of FFR value more than 0.8, non-IRA lesion wll be deferred without PCI. If FFR value was equal or less than 0.8, non-IRA lesion will be revascularized.

干预措施: Staged in-hospital complete revascularization

Immediate CR (complete revascularization)

Non-infarct related artery (IRA) will be revascularized immediately after percutaneous coronary intervention (PCI) for IRA (during index PCI). Non-IRA lesion which have equal or more than 70% diameter stenosis by visual estimation will be revascularized without fractional flow reserve (FFR) evaluation. Non-IRA lesion with diameter stenosis 50-69% by visual estimation will be evaluated using FFR device. In case of FFR value more than 0.8, non-IRA lesion wll be deferred without PCI. If FFR value was equal or less than 0.8, non-IRA lesion will be revascularized.

干预措施: Immediate complete revascularization

结局指标

主要结局

Cumulative incidence rate of all-cause death, non-fatal myocardial infarction, or all unplanned revascularization

时间窗: Up to 12 months

Composite endpoint of all-cause death, non-fatal myocardial infarction, or all unplanned revascularization at 1 year from baseline

次要结局

  • Cumulative incidence rate of target-lesion revascularization(Up to 12 months)
  • Cumulative incidence rate of hospitalization for unstable angina(Up to 12 months)
  • Rate of contrast-induced nephropathy(Up to 12 months)
  • Cumulative incidence rate of non-cardiac death(Up to 12 months)
  • Cumulative incidence rate of ischemic and hemorrhagic stroke(Up to 12 months)
  • Cumulative incidence rate of target-vessel revascularization(Up to 12 months)
  • Cumulative incidence rate of non-target vessel revascularization(Up to 12 months)
  • Cumulative incidence rate of definite or probable stent thrombosis(Up to 12 months)
  • Cumulative incidence rate of all-cause death(Up to 12 months)
  • Cumulative incidence rate of non-fatal myocardial infarction(Up to 12 months)
  • Cumulative incidence rate of hospitalization for heart failure(Up to 12 months)
  • Cumulative incidence rate of major bleeding (BARC [Bleeding Academic Research Consortium] definitions type 3 or 5)(Up to 12 months)
  • Cumulative incidence rate of all unplanned revascularization(Up to 12 months)
  • Cumulative incidence rate of cardiac death(Up to 12 months)

研究点 (2)

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