Vascular Evaluation for Revascularization: Defining the Indications for Coronary Therapy: A Pilot Study (VERDICT)
A Prospective, Global, Multicenter, Non-Randomized, Non-Blinded Study in Patients With Intermediate Coronary Lesions to Examine the Correlation Between Fractional Flow Reserve (FFR) and Intravascular Ultrasound With Virtual Histology (VH-IVUS)
研究概览
研究类型
注册 (实际的)
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Patient-specific inclusion criteria:
- Clinical presentation: stable angina, unstable angina, non-ST segment-elevation myocardial infarction (NSTEMI) (Braunwald classification of unstable angina, see Attachment 2) or recent STEMI (>48 hours before enrollment).
- Patient is scheduled for coronary catheterization with or without percutaneous coronary intervention.
- Age ≥18 years.
- Patient is able to read, understand, and sign the informed consent document.
- Patient agrees to all protocol related procedures, including follow-up through 3 years.
Lesion-specific inclusion criteria:
- The patient has at least one intermediate coronary lesion to be assessed by FFR and VH-IVUS, defined as a lesion with a visually-estimated diameter stenosis ≥40% to <80% with a visually-estimated angiographic reference segment diameter of 2.75 mm - 4.0 mm.
- There may only be one study lesion in the major epicardial coronary artery or its branches. All other stenosis in this epicardial coronary artery or its branches must be <40% by visual angiographic assessment. E.g.., if the lesion is in the Left Anterior Descending(LAD), there may be no other significant lesions (≥40%) in the LAD, septals or diagonal branches. A single lesion may have normal or nearly normal appearing segments within the lesion as long as it is contained within one CASS segment. Moreover, a single lesion may span two or more CASS segments as long as there is no normal or nearly normal appearing segments >5mm in length within the lesion. However, if a diseased lesion extends across two or more CASS segments and has one or more >5 mm lengths of normal or nearly normal appearing segments within the lesion, then it is considered 2 separate lesions, and may not be enrolled.
- More than 1 intermediate lesion per patient may be enrolled, as long as each lesion meets the entry criteria as a study lesion (e.g. one intermediate lesion in 1, 2 or 3 unique epicardial coronary arteries (LAD vs. LCX vs. RCA), with FFR and VH-IVUS performed in each vessel. Thus, up to 3 lesions may be enrolled per patient (one in each major epicardial coronary artery).
- PCI of any lesion in the target vessel (the main epicardial coronary artery or any of its branches) may not have been performed in the preceding 1 year (including during the index procedure) and may not be planned within the next 1 year.
Patients undergoing PCI of non-study lesions in non-study target vessels during the index procedure may be enrolled if one or more qualifying intermediate lesion is otherwise present in a different epicardial vessel, but PCI of all non-study lesions must be performed first (including staged procedures) and must be successful and uncomplicated before formal enrollment into this study. The PCI cannot occur in the epicardial coronary artery or its branches containing the intermediate lesion.
- Successful PCI is defined as residual diameter stenosis of <50% in all treated lesions with Thrombolysis in Myocardial Infarction (TIMI) -3 flow in all treated vessels.
- Uncomplicated PCI is defined as the absence of intra-procedural chest pain or ST-segment changes lasting >10 minutes, sustained vessel closure, slow or no reflow, side branch loss, distal embolization, perforation, residual dissection (>type B), or requirement for cardiopulmonary resuscitation, cardioversion or defibrillation, pacemaker insertion, intubation, intra-aortic balloon insertion or intravenous pressors.
Patient-specific exclusion criteria:
- Prior CABG at any time.
- The patient is likely to undergo PCI, CABG or other cardiac surgical procedure within 1 year of the procedure.
- ST-segment elevation myocardial infarction within 48 hours of the procedure.
- Cardiogenic shock defined as systolic blood pressure <90 mmHg lasting >30 minutes, not responding to intravenous fluids, and/or requiring intravenous pressors or an intra-aortic balloon pump or other hemodynamic support device.
- Heart failure as defined by New York Heart Association class III or IV (see Attachment 2).
- Respiratory failure requiring intubation or supplementary oxygen.
- Left ventricular ejection fraction <30% as determined by 2D echo, nuclear testing, magnetic resonance imaging (MRI), or left ventriculography.
- Any moderate or severe cardiac valve disease.
- Cerebrovascular accident or transient ischemic attack (TIA) within the past 60 days, or any permanent neurologic deficit.
- Chronic renal insufficiency (serum creatinine > 2.5mg/dl).
- History of drug abuse or alcohol abuse or any other condition making it unlikely that the patient will comply with all study procedures, including follow-up for 3 years
- Any condition with expected survival <2 years.
- Pregnant or nursing patients and those who plan pregnancy in the period up to 1 year following the index procedure. Female patients of child-bearing potential must have a negative pregnancy test done within 7 days prior to the index procedure.
- Patients currently participating in another study of an investigational drug or device which has not yet reached its primary endpoint.
- Oral intake by the patient of any caffeinated beverage within 4 hours of the procedure
- Use within 12 hours of theophylline, aminophylline or any xanthine derivative.
Lesion-specific exclusion criteria:
- An unprotected left main coronary stenosis is present (visually assessed %DS ≥40%, whether or not requiring treatment). The study lesion cannot be a left main lesion.
- The intermediate lesion is in a vessel with thrombus, moderate or severe calcification, angulation, or tortuosity. PCI may be performed in such non target vessels or lesions prior to study enrollment, however, as long as successful and uncomplicated, after which the patient is enrolled in the study.
- The study lesion is an ostial lesion (within 5 mm of the aorta or the distal left main coronary artery) or is bifurcation lesion requiring planned dual stenting.
学习计划
研究是如何设计的?
设计细节
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
---|---|
The concordance between FFR and IVUS minimum lumen area(MLA) as assessed by continuous correlation (regression), categorical cutoff values , and being unadjusted and adjusted for lesion length, %plaque burden(PB) and VH-thin capped Fibro Atheroma(TCFA)
大体时间:3 year
|
3 year
|
次要结果测量
结果测量 |
大体时间 |
---|---|
The concordance between operator assessed % diameter stenosis(DS), core lab assessed %DS, FFR and MLA in intermediate lesions
大体时间:3 year
|
3 year
|
Operator assessed and core lab assessed angiographic %DS, and VH-IVUS MLA, lesion length, %PB, and plaque types in intermediate lesions, with core lab assessment as the reference
大体时间:3 year
|
3 year
|
FFR and VH-IVUS derived MLA, %PB, lesion length, and plaque type in deferred vs. treated lesions
大体时间:3 year
|
3 year
|
Operator revascularization decisions (deferral vs. PCI/coronary artery bypass graft(CABG)) according to operator assessed angiographic %DS, FFR and VH-IVUS results in intermediate coronary lesions
大体时间:3 year
|
3 year
|
Deferred study lesion clinical event rates up to three years according to %DS, FFR and VH-IVUS, and comparison with treated study lesion clinical event rates up to three years
大体时间:3 year
|
3 year
|
Treated study lesion clinical event rates up to three years and their correlation with index FFR and VH-IVUS pre and post stenting
大体时间:3 year
|
3 year
|
合作者和调查者
调查人员
- 首席研究员:Gregg W Stone, MD、Columbia University
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
FFR and VH-IVUS的临床试验
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Instituto Dante Pazzanese de CardiologiaFundação de Amparo à Pesquisa do Estado de São Paulo招聘中
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S.M. Misericordia HospitalSan Giovanni Addolorata Hospital未知
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Seoul National University HospitalInje University完全的
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Vilnius University Hospital Santaros KlinikosVilnius University完全的
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Seoul National University HospitalSamsung Medical Center, Sungkyunkwan University School of Medicine; Ulsan University Hospital; Second Affiliated Hospital, School of Medicine, Zhejiang University 和其他合作者未知
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Vilnius University Hospital Santaros KlinikosVilnius University完全的心肌梗塞 | 心肌缺血 | 冠状动脉疾病