The ASSURE ROT Registry: Bioresorbable Vascular Scaffold Following Rotablation for Complex Coronary Lesions (ASSURE ROT)
Postmarketing Surveillance Registry to Monitor Everolimus-eluting Bioresorbable Vascular Scaffold Following Rotational Atherectomy for the Treatment of Complex Coronary Lesions - The ASSURE ROT Registry
調査の概要
詳細な説明
研究の種類
入学 (予想される)
連絡先と場所
研究場所
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Hamburg、ドイツ、22391
- 募集
- Medical Care Center Prof. Mathey, Prof. Schofer GmbH
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コンタクト:
- Detlef G Mathey, Prof. Dr.
- 電話番号:152 +4940889009
- メール:dgmathey@web.de
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副調査官:
- Joachim Schofer, Prof. Dr.
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副調査官:
- Carsten Schwencke, PD Dr.
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
The recommendation to implant BVS in an individual patient in whom rotational atherectomy of a complex target lesion has been conducted, 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 complex de novo native coronary artery lesions
- Patients with evidence of myocardial ischemia
Regarding to lesion
- Reference vessel diameter ≥ 2.5 mm and ≤ 3.8 mm, visually estimated or by online QCA
- Percent diameter stenosis ≥ 50% and < 100%, visually estimated or 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
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 noncompliance 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
Target lesion(s) meets none of the following criteria:
- 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
- Ostial lesion > 40% stenosed by visual estimation or side branch requiring predilation
- Excessive tortuosity proximal to or within the lesion (extreme angulation proximal to or within the lesion)
- Restenotic from previous intervention
Target vessel is not containing thrombus
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 観測モデル:コホート
- 時間の展望:見込みのある
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Major Adverse Cardiac Event (MACE)
時間枠: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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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Acute procedural success
時間枠: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
時間枠: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
時間枠:At time of intervention, and at 6, 12, 24, and 36 months
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At time of intervention, and at 6, 12, 24, and 36 months
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Cardiac death
時間枠:At time of intervention, and at 6, 12,24, and 36 months
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At time of intervention, and at 6, 12,24, and 36 months
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Myocardial infarction
時間枠:At time of intervention, and at 6, 12, 24, and 36 months
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At time of intervention, and at 6, 12, 24, and 36 months
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Ischemia driven target lesion revascularisation (TLR)
時間枠:At time of intervention, participants will be followed for the duration of hospital stay (an expected average of 3 days), at 6, 12, 24, and 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, 24, and 36 months
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Ischemia driven target vessel revascularisation (TVR)
時間枠:at 6, 12, 24, and 36 month
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at 6, 12, 24, and 36 month
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In-lesion % diameter stenosis
時間枠:Baseline and final at time of intervention and at 24 months FU
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QCA: Independent CoreLab
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Baseline and final at time of intervention and at 24 months FU
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Minimal lumen diameter (MLD)
時間枠:Baseline and final at time of intervention and at 24 months FU
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QCA: Independent CoreLab
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Baseline and final at time of intervention and at 24 months FU
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In-scaffold late lumen loss (LLL)
時間枠:At 24 months FU
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At 24 months FU
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協力者と研究者
捜査官
- 主任研究者:Detlef G Mathey, Prof. Dr.、Medical Care Center Prof. Mathey, Prof. Schofer GmbH
出版物と役立つリンク
一般刊行物
- 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.
- Basavarajaiah S, Naganuma T, Latib A, Colombo A. Can bioabsorbable scaffolds be used in calcified lesions? Catheter Cardiovasc Interv. 2014 Jul 1;84(1):48-52. doi: 10.1002/ccd.24939. Epub 2013 Aug 31.
- Patel N, Banning AP. Bioabsorbable scaffolds for the treatment of obstructive coronary artery disease: the next revolution in coronary intervention? Heart. 2013 Sep;99(17):1236-43. doi: 10.1136/heartjnl-2012-303346. Epub 2013 Mar 8.
研究記録日
主要日程の研究
研究開始
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。