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临床试验/NCT02057900
NCT02057900已完成1 期

Transplantation of Human Embryonic Stem Cell-derived CD15+ Isl-1+ Progenitors in Severe Heart Failure

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2013年5月27日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
10
试验地点
2
主要终点
number and nature of adverse events

研究概览

简要总结

The purpose of the study is to assess the feasibility and safety of a transplantation of cardiac-committed progenitor cells derived from human embryonic stem cells in patients with severe heart failure.

详细描述

Heart failure due to coronary artery disease is a major problem because of its high prevalence, increased incidence and associated costs. When conventional medical/interventional treatments fail and if cardiac transplantation is contra-indicated, alternate options need to be considered. Transplantation of stem cells has emerged as one of them. While the optimal cell type still remains debatable, there is compelling evidence that cells whose phenotype closely matches that of the recipient tissue look sound candidates. In this context, human embryonic stem cells are attractive because of the possibility to drive their fate in vitro, prior to transplantation, towards a cardiac phenotype. We have developed a process for achieving such a commitment and generating cardiac-directed cells. The objective of this study is to assess both the feasibility and safety of this approach. In addition, the disadvantages of multiple intramyocardial injections have now been recognized. We have then taken advantage of the surgical setting of the trial (which entails concomitant coronary artery bypass or a mitral valve procedure) to switch from injections to the epicardial delivery of a fibrin gel into which the progenitor cells have been embedded. Coverage of this cell-loaded patch by an autologous pericardial flap is finally designed to provide trophic factors to the underlying cellular graft with the hope of improving its viability.

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
18 Years 至 81 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 and less than 81 years
  • Severe left ventricular systolic dysfunction with left ventricular ejection fraction (LVEF) ≤ 35% as assessed by echocardiography or scintigraphy
  • History of myocardial infarction (older than 6 months) with a residual akinesia involving more than 2 (out of 16) contiguous segments, as assessed by basal echocardiography
  • New York Heart Association (NYHA) Class III or IV despite optimal standard of care including diuretics and angiotensin receptor blockers and, if possible, beta blockers and aldosterone blockers
  • Previous implantation of an automatic internal defibrillator associated, whenever indicated, to ventricular resynchronization
  • Indication for a conventional cardiac surgical procedure : coronary artery bypass grafting involving, or not, the infarct area planned to be covered by the cell-loaded patch or mitral valve repair or replacement for ischemic mitral valve regurgitation; Non Eligibility to heart transplantation; Affiliation to a social security regimen
  • Willingness and ability to give written informed consent

排除标准

  • Pregnant or potentially child-bearing women
  • Patients with poor echogenicity
  • Left ventricular aneurysm
  • Contra-indication to immunosuppressive drugs (history of cancer, infections like B or C hepatitis, positivity for Hepatitis-B, HIV, HTLV1)
  • Contra-indication to sternotomy
  • Alloimmunisation against the cell line from which the progenitors are derived
  • Cardiogenic shock or NYHA Class IV heart failure requiring need for intravenous drugs
  • Intellectual deterioration or psychiatric disease interfering with the ability to obtain an informed consent and to achieve a close follow-up of the patient
  • Noncardiac disease which may reduce life expectancy in the short term
  • Simultaneous participation to another trial

研究组 & 干预措施

Human embryonic stem cell

Experimental

Patients with ischemic heart failure receiving a fibrin gel embedding human embryonic stem cell-derived CD15+ Isl-1+ progenitors in addition to coronary artery bypass grafting and/or a mitral valve procedure.

干预措施: Human embryonic stem cell-derived CD15+ Isl-1+ progenitors (Biological)

结局指标

主要结局

number and nature of adverse events

时间窗: Within the first year after surgery

Evidence for new clinical/biological abnormalities, occurrence of arrhythmias or development of a cardiac or extra-cardiac tumor.

次要结局

  • Feasibility of patch's generation and its efficacy on cardiac functions(Within the first year after surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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