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首页> 外文期刊>The American heart journal >Rationale and design for TIME: A phase II, randomized, double-blind, placebo-controlled pilot trial evaluating the safety and effect of timing of administration of bone marrow mononuclear cells after acute myocardial infarction.
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Rationale and design for TIME: A phase II, randomized, double-blind, placebo-controlled pilot trial evaluating the safety and effect of timing of administration of bone marrow mononuclear cells after acute myocardial infarction.

机译:TIME的理由和设计:一项II期,随机,双盲,安慰剂对照的试验性研究,评估了急性心肌梗塞后给药骨髓单核细胞的时机和安全性。

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Several previous studies have demonstrated that administration of autologous bone marrow-derived mononuclear cells (BMMNCs) improves cardiac function in patients after acute myocardial infarction (AMI). However, optimum timing of administration has not been investigated in a clinical trial. The Cardiovascular Cell Therapy Research Network was developed and funded by the National Heart, Lung, and Blood Institute to address important questions such as timing of cell delivery and to accelerate research in the use of cell-based therapies. The TIME trial is a randomized, phase II, double-blind, placebo-controlled clinical trial. The 5 member clinical sites of the Cardiovascular Cell Therapy Research Network will enroll 120 eligible patients with moderate-to-large anterior AMIs who have undergone successful percutaneous coronary intervention of the left anterior descending coronary artery and have a left ventricular (LV) ejection fraction
机译:先前的几项研究表明,自体骨髓源性单核细胞(BMMNC)的使用可改善急性心肌梗塞(AMI)患者的心脏功能。但是,尚未在临床试验中研究最佳给药时间。心血管细胞治疗研究网络是由美国国立心肺血液研究所开发和资助的,旨在解决重要的问题,例如细胞递送的时机,并加速基于细胞疗法的使用研究。 TIME试验是一项随机,II期,双盲,安慰剂对照的临床试验。心血管细胞治疗研究网络的5个成员临床站点将招募120名符合条件的中至大型前AMI的患者,这些患者已成功地对左冠状动脉前降支进行了经皮冠状动脉介入治疗,并且左心室(LV)射血分数< / = 45%超声心动图检查。在AMI后第3天或第7天,参加者将进行150 x 10(6)BMMNC的骨髓穿刺和冠状动脉内输注或安慰剂。这项研究的目的是(1)通过心脏磁共振成像在6个月时评估急性心肌梗死患者与安慰剂治疗相比,BMMNCs对区域和整体LV功能的影响;以及(2)评估BMMNC输注是否对急性心肌梗死有影响全球和区域左室功能和安全性受管理时间的影响。这项研究将为AMI和经皮冠状动脉介入治疗后高危患者自体BMMNC治疗的临床可行性和适当时机提供进一步的见解。

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