ABSORB: Postmarketing Surveillance Registry to Monitor the Everolimus-eluting Bioresorbable Vascular Scaffold in Patients With Coronary Artery Disease (ASSURE)
2016年12月8日 更新者:Detlef Mathey、Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.
ABSORB: Initial Clinical Experience With the Everolimus-eluting Bioresorbable Vascular Scaffold (BVS) System in the Treatment of de Novo Native Coronary Artery Lesions - a Surveillance Registry
The registry aims to evaluate the safety, performance and efficacy of the Everolimus-eluting bioresorbable vascular scaffold (BVS) system in patients with de novo native coronary artery lesions in all-day clinical practice.
研究概览
详细说明
Bioresorbable scaffolds are transient implants.
They act like drug-eluting metallic stents (DES) during the first 3 months by supporting the vessel wall thereby keeping the artery patent.
Subsequently, resorption of the scaffold begins and its structure loosens.
As a result of everolimus release, neointimal growth is inhibited similar to DES.
Finally the implant is reabsorbed completely in about 2-3 years.
BVS in terms of late stent thrombosis may be safer than DES.
Transiently scaffolded vessels may regain their natural curvature and angulation as well as response to nitroglycerine and endothelial function.
研究类型
观察性的
注册 (实际的)
183
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Bernau、德国、16321
- Herzzentrum Brandenburg in Bernau
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Coburg、德国、96450
- Klinikum Coburg GmbH
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Essen、德国、45138
- Elisabeth-Krankenhaus Essen GmbH
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Hamburg、德国、22527
- Medical Care Center Prof. Mathey, Prof. Schofer GmbH
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Kiel、德国、24105
- Universitatsklinikum Schleswig-Holstein
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Ulm、德国、89081
- Universitätsklinikum Ulm
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 75年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
取样方法
概率样本
研究人群
Patients with cardiovascular disease
描述
The recommendation to implant BVS in an individual patient is purely based on clinical grounds. These are determined by the instructions for use (IFU) of the BVS and by the clinical experience accumulated so far from clinical studies.These studies suggest that the BVS should be implanted under certain conditions, which are determined by the patient and the coronary lesion treated:
Eligible:
Regarding to patient
- Patient ≥ 18 and ≤ 75 years with a live expectancy of at least 5 years with ischemic heart disease (chronic, NSTEMI and unstable angina) due to one or more de novo native coronary artery lesions
- Patients with evidence of myocardial ischemia
Regarding to lesion
- Reference vessel diameter ≥ 2.0 mm and ≤ 3.8 mm, visually estimated and by online QCA
- Percent diameter stenosis ≥ 50% and < 100%, visually estimated and by online QCA
- TIMI ≥1
- Previous interventions of target vessel lesions should have been done ≥ 6 months prior to index procedure and > 10 mm distal to the target lesion
- Previous interventions of non-target vessel lesions should have been done ≥ 30 days prior to index procedure
- In case of >1 target lesions, those should be from different epicardial vessels
Not eligible:
Regarding to patient
- Patient in whom antiplatelet therapy and/or anticoagulant therapy is contraindicated
- Patient with a known hypersensitivity or contraindication to aspirin, both heparin and bivalirudin, clopidogrel, ticlopidine, prasugrel and ticagrelor, everolimus, poly (L-lactide), poly (D,L-lactide), or platinum, or with contrast sensitivity, who cannot be adequately premedicated
- Patient has a known diagnosis of acute myocardial infarction (STEMI) within 72 hours preceding the index procedure and CK and CK-MB have not returned within normal limits at the time of procedure
- Patient is currently experiencing clinical symptoms consistent with STEMI
- Patient has current unstable arrhythmias
- Patient has a known left ventricular ejection fraction < 30%
- Patient has received a heart transplant or any other organ transplant or is waiting for any organ transplant
- Patient receiving or scheduled to receive chemotherapy for malignancy within 30 days prior to or after procedure
- Patient is receiving immunosuppression therapy and has known immunosuppressive or autoimmune disease
- Patient is receiving or scheduled to receive chronic anticoagulation therapy
- Elective surgery is planned within the first 6 month after the procedure that will require discontinuing either aspirin or clopidogrel
- Patient has a platelet count < 100 000 cells/mm3 or > 700 000 cells/mm3, a WBC of
- < 3000 cells/mm3, or documented or suspected liver disease
- Patient has known renal insufficiency
- Patient has a history of bleeding diathesis or coagulopathy or will refuse blood transfusions
- Patient has cerebrovascular accident or transient ischemic neurological attack within the past six month
- Patient has had a significant GI or urinary bleed within the past six months
- Patient has extensive peripheral vascular disease that precludes safe 6 French sheath insertion
- Patient has other medical illness (e.g., cancer or congestive heart failure) or known history of substance abuse (alcohol, cocaine, heroin etc.) that may cause non.compliance with the clinical study plan, confound the data interpretation or is associated with a limited life expectancy (i.e., les than one year)
- Women of childbearing potential who have not undergone surgical sterilization or are not post-menopausal
Regarding to lesion
- Aorto-ostial location
- Left main location
- Located within 2 mm of the origin of LAD or LCX
- Located within an arterial or saphenous vein graft or distal to a diseased (defined as vessel irregularity per angiogram and > 20% stenosed lesion by visual estimation) arterial or saphenous vein graft
- Lesion involving a bifurcation with side branch vessel ≥ 2 mm in diameter, ostial lesion > 40% stenosed by visual estimation or side branch requiring predilation
- Total occlusion (TIMI flow 0), prior to wire passing
- Excessive tortuosity proximal to or within the lesion (extreme angulation (≥ 90°) proximal to or within the lesion)
- Heavy calcification
- Restenotic from previous intervention
- Target vessel is containing thrombus
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 观测模型:队列
- 时间观点:预期
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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(This trial has no primary outcome, all outcomes are of equal weight), Major Adverse Cardiac Event (MACE)
大体时间:at 24 months
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Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardiac death
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at 24 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Acute procedural success
大体时间:At the end of hospital stay (maximum of 7 days)
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Achievement of final in-scaffold residual stenosis of < 50% and TIMI flow 3 of the target site.
Successful delivery and deployment of at least one study scaffold at the intended target lesion and successful withdrawal of the delivery system for all target lesions without occurrence of cardiac death, target vessel MI or repeat TLR during hospital stay (maximum of 7 days).
In dual target lesion setting both lesions must meet clinical procedure success criteria.
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At the end of hospital stay (maximum of 7 days)
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Acute device success
大体时间:At time of intervention
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Successful delivery and deployment of the first scaffold at the intended target lesion (in overlapping setting both planned scaffolds) and successful withdrawal of delivery system.
Attainment of < 50 % residual stenosis and TIMI flow 3 of the target site, using the BVS without the need for other non- study stents.
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At time of intervention
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Scaffold thrombosis
大体时间:At time of intervention, and at 6, 12, 24, 36 months
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At time of intervention, and at 6, 12, 24, 36 months
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Cardiac death
大体时间:At time of intervention, and at 6, 12,24, 36 months
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At time of intervention, and at 6, 12,24, 36 months
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Myocardial infarction
大体时间:At time of intervention, and at 6, 12, 24 36 months
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At time of intervention, and at 6, 12, 24 36 months
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Ischemia driven target lesion revascularisation (TLR)
大体时间:At time of intervention, and at 6, 12, 24, 36 months
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Target lesion denominates scaffolded segment and 5 mm beyond.
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At time of intervention, and at 6, 12, 24, 36 months
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Major Adverse Cardiac Event (MACE)
大体时间:At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 36 months
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Composite of ischemia driven target lesion revascularisation (TLR), myocardial infarction and cardial death
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At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 36 months
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Ischemia driven target vessel revascularisation (TVR)
大体时间:at 6, 12, 24, 36 months
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TVR is ischemia driven.
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at 6, 12, 24, 36 months
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Ischemia driven target vessel failure (TVF)
大体时间:at 6, 12, 24, 36 month
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at 6, 12, 24, 36 month
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In-lesion % diameter stenosis
大体时间:Prior procedure
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Prior procedure
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In-scaffold % diameter stenosis
大体时间:At time of intervention and at angiographic FU if applicable
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At time of intervention and at angiographic FU if applicable
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Minimal lumen diameter (MLD)
大体时间:Prior and post procedure and at FU if applicable
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Prior and post procedure and at FU if applicable
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In-scaffold late lumen loss (LLL)
大体时间:At angiographic follow-up if applicable
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At angiographic follow-up if applicable
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Proximal and distal late lumen loss (LLL)
大体时间:At angiographic follow-up if applicable
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At angiographic follow-up if applicable
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In-lesion late lumen loss
大体时间:At angiographic follow-up if applicable
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At angiographic follow-up if applicable
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Response to nitroglycerin
大体时间:Before scaffold implantation, during angiographic follow-up if applicable
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Before scaffold implantation, during angiographic follow-up if applicable
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In-lesion angiographic binary restenosis (≥ 50%)
大体时间:At angiographic follow-up if applicable
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At angiographic follow-up if applicable
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Curvature (cm-1)
大体时间:Prior and post procedure and at angiographic follow-up if applicable
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treated region
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Prior and post procedure and at angiographic follow-up if applicable
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Angulation (°)
大体时间:Prior and post procedure and at angiographic follow-up if applicable
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Treated region
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Prior and post procedure and at angiographic follow-up if applicable
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Clinical success
大体时间:At time of intervention, and at 6, 12, 24, 36 months
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Procedural success and freedom from TVF, TVR, CABG and scaffold thrombosis
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At time of intervention, and at 6, 12, 24, 36 months
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Coronary artery bypass grafting (CABG)
大体时间:at 6, 12, 24, 36 month
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at 6, 12, 24, 36 month
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Detlef G Mathey, MD、Medical Care Center Prof. Mathey, Prof. Schofer GmbH
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Serruys PW, Onuma Y, Dudek D, Smits PC, Koolen J, Chevalier B, de Bruyne B, Thuesen L, McClean D, van Geuns RJ, Windecker S, Whitbourn R, Meredith I, Dorange C, Veldhof S, Hebert KM, Sudhir K, Garcia-Garcia HM, Ormiston JA. Evaluation of the second generation of a bioresorbable everolimus-eluting vascular scaffold for the treatment of de novo coronary artery stenosis: 12-month clinical and imaging outcomes. J Am Coll Cardiol. 2011 Oct 4;58(15):1578-88. doi: 10.1016/j.jacc.2011.05.050.
- Dudek D, Onuma Y, Ormiston JA, Thuesen L, Miquel-Hebert K, Serruys PW. Four-year clinical follow-up of the ABSORB everolimus-eluting bioresorbable vascular scaffold in patients with de novo coronary artery disease: the ABSORB trial. EuroIntervention. 2012 Jan;7(9):1060-1. doi: 10.4244/EIJV7I9A168.
- Diletti R, Onuma Y, Farooq V, Gomez-Lara J, Brugaletta S, van Geuns RJ, Regar E, de Bruyne B, Dudek D, Thuesen L, Chevalier B, McClean D, Windecker S, Whitbourn R, Smits P, Koolen J, Meredith I, Li D, Veldhof S, Rapoza R, Garcia-Garcia HM, Ormiston JA, Serruys PW. 6-month clinical outcomes following implantation of the bioresorbable everolimus-eluting vascular scaffold in vessels smaller or larger than 2.5 mm. J Am Coll Cardiol. 2011 Jul 12;58(3):258-64. doi: 10.1016/j.jacc.2011.02.052.
- Gomez-Lara J, Brugaletta S, Farooq V, van Geuns RJ, De Bruyne B, Windecker S, McClean D, Thuesen L, Dudek D, Koolen J, Whitbourn R, Smits PC, Chevalier B, Morel MA, Dorange C, Veldhof S, Rapoza R, Garcia-Garcia HM, Ormiston JA, Serruys PW. Angiographic geometric changes of the lumen arterial wall after bioresorbable vascular scaffolds and metallic platform stents at 1-year follow-up. JACC Cardiovasc Interv. 2011 Jul;4(7):789-99. doi: 10.1016/j.jcin.2011.04.009.
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2012年4月1日
初级完成 (实际的)
2013年3月1日
研究完成 (实际的)
2016年6月1日
研究注册日期
首次提交
2012年4月17日
首先提交符合 QC 标准的
2012年4月20日
首次发布 (估计)
2012年4月24日
研究记录更新
最后更新发布 (估计)
2016年12月9日
上次提交的符合 QC 标准的更新
2016年12月8日
最后验证
2016年12月1日
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.