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临床试验/NCT02851758
NCT02851758招募中不适用

Transplantation of Autologously Derived Mitochondria for Protection Against Ischemia-reperfusion Injury Following Ischemia in Subjects on ECMO Support

Boston Children's Hospital1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2017年8月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
16
试验地点
1
主要终点
Safety- Incidence of severe adverse events

研究概览

简要总结

The investigators propose a robust therapeutic intervention to ameliorate myocardial ischemia/ reperfusion injury and significantly decrease morbidity and mortality in patients requiring extracorporeal membrane oxygenation (ECMO), by direct injection of autogeneic mitochondria into the ischemic myocardium.

详细描述

Autologous mitochondria will be delivered to the ischemic heart muscle in one of two ways, during clinically indicated surgical procedure or during clinically indicated cardiac catheterization.

For surgical re-operation subjects:

After the subject's chest is open, 1-2 6mm biopsies will be collected from the exposed skeletal muscle of the chest wall. The tissue will be processed at bedside to extract the autologous mitochondria. Surgery will proceed as clinically indicated. Prior to closure of the chest, autologous mitochondria will be injected via 5-10 injections of approximately 0.1 mL each to the damaged area (if damaged muscle is local) or via injection into the proximal aorta while cross-clamped for clinically indicated surgery for global distribution of mitochondria via the coronary arteries if there is no evident area of damage. Following completion of surgical maneuvers the mitochondria will be injected into the aorta and the cross-clamp will be removed. If there is global injury but a cross-clamp is not clinically indicated, direct injection into the myocardium will occur throughout the ventricle as previously described. Chest closure will then occur as and if clinically indicated for both techniques.

For catheterization subjects:

Once in the catheterization lab, the temporary chest closure will be removed and 1-2 6 mm biopsies will be collected from the exposed skeletal muscle of the chest wall by the cardiac surgery team. The tissue will be processed at bedside to extract the autologous mitochondria. The catheterization will proceed as clinically indicated. Prior to completion of the procedure (interventional to restore blood flow or hemodynamics), mitochondria will be infused in 5 mL of buffer as conducted in large animal studies (5) via intracoronary infusion followed by a 5 mL flush with normal saline. Total dose of mitochondria will be equal to direct injection subjects, with a larger dilution to allow to infusion via cardiac catheter.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Pediatric cardiology patients under the age of 18 on ECMO
  • concerns for ischemic injury on the Cardiac Intensive Care Unit

排除标准

  • Known mitochondria disorders

结局指标

主要结局

Safety- Incidence of severe adverse events

时间窗: 1 week

Subjects will be SAE free for one week following injection

次要结局

  • Efficacy- Improvement in Outcome measures: ability to be separated from ECMO support, measured in days since injection(1 week- 1 month)
  • Efficacy- Improvement in Outcome measures: increased ventricular function on echocardiogram, measured by ejection fraction(1 week- 1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sitaram Emani

Principal Investigator

Boston Children's Hospital

研究点 (1)

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