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临床试验/NCT01956708
NCT01956708已完成不适用

Transfer of Cardioprotection During Remote Ischemic Conditioning

University Hospital, Essen2 个研究点 分布在 1 个国家目标入组 392 人开始时间: 2013年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
392
试验地点
2
主要终点
Myocardial protection

研究概览

简要总结

Remote ischemic preconditioning (RIPC) with transient upper limb ischemia/reperfusion provides peri-operative myocardial protection, is safe and improves prognosis in patients undergoing elective CABG surgery.

The signal transfer from limb to heart is unknown. Thus, the aim of this study is to identify the pathways which transfer the cardioprotective signal from the ischemic/reperfused extremity to the heart in humans undergoing surgical coronary revascularization.

详细描述

The investigators will obtain arterial blood samples before skin incision and 1-72 h after the remote ischemic preconditioning protocol and analyze them biochemically. The investigators focus on those ligands that have been previously implicated in conditioning protocols at any organ. In addition, the investigators will use a bioassay system, consisting of a Langendorff-perfused isolated heart with coronary occlusion/reperfusion and infarct size by TTC staining as endpoint, and then expose this bioassay system to arterial plasma obtained after the remote ischemic preconditioning stimulus or placebo. This approach will allow us to further characterize any potential transfer signal candidate with a pharmacological antagonist approach.

The investigators will also obtain human atrial appendages after the remote ischemic preconditioning protocol or placebo and before patients were connected to the extracorporeal circulation. Contractile function of isolated trabeculae and vasomotor function of isolated arterial vessels will be analyzed in a bioassay system.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Consecutive patients > 18 years after written informed consent
  • elective, isolated CABG surgery with and without valvuloplastic surgery
  • two-stage cannulation, cardiopulmonary bypass
  • antegrade Bretschneider cardioplegia
  • mild hypothermia (32°C)
  • preoperative standard medication (statins, betablocker, aspirin)
  • standard anesthesia (see above)
  • intraoperative standard protocol (full heparinization with ACT, aprotinin, protamin)
  • postoperative standard protocol (500 mg aspirin after 2 h, low-dose heparin after 4 h)

排除标准

  • preoperative
  • prior percutaneous coronary intervention (PCI) within 6 weeks
  • any preoperative troponin T elevation
  • renal insufficiency (creatinine >200 µmol/l)
  • reoperation
  • emergency surgery
  • acute coronary syndrome (unstable angina, STEMI, NSTEMI) within 4 weeks
  • dual anti-platelet therapy (clopidogrel+aspirin)
  • intraoperative
  • harvesting of a. radialis
  • coronary thrombendarterectomy
  • complications (bypass-low flow/ -occlusion)
  • antithrombotic therapy (intraoperative clopidogrel + aspirin)
  • retrograde cardioplegia

结局指标

主要结局

Myocardial protection

时间窗: 72 h, postoperatively

Cumulative postoperative troponin T release

次要结局

  • All-cause mortality(30 days and 1 year after CABG surgery and after complete follow-up)
  • MACCE(30 days and 1 year after CABG surgery after complete follow-up)
  • renal function(72 h, postoperatively)
  • Cardioprotective factors released into circulating blood(before skin incision versus 1-72 h after RIPC)
  • Myocardial function in vitro(after RIPC)

研究者

发起方
University Hospital, Essen
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Dr. med. Markus Kamler

Prof. Dr. med. Markus Kamler

University Hospital, Essen

研究点 (2)

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