首页> 外文期刊>Journal of cardiovascular translational research >Double-blind parallel placebo-controlled study to evaluate the effect of molsidomine on the endothelial dysfunction in patients with stable angina pectoris undergoing percutaneous coronary intervention: The MEDCOR trial
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Double-blind parallel placebo-controlled study to evaluate the effect of molsidomine on the endothelial dysfunction in patients with stable angina pectoris undergoing percutaneous coronary intervention: The MEDCOR trial

机译:评估莫西度明对接受经皮冠状动脉介入治疗的稳定型心绞痛患者内皮功能障碍影响的双盲平行安慰剂对照研究:MEDCOR 试验

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摘要

The effects of molsidomine (a direct nitric oxide donor) on the endothelial dysfunction have never been evaluated using reactive hyperemia peripheral arterial tonometry (RH-PAT). The objective of the MEDCOR double-blind trial will be to demonstrate the superiority of molsidomine (Coruno? 16 mg, once daily) over placebo, on improving the endothelial function (Endoscore by RH-PAT) after 12 months of treatment in stable angina patients undergoing elective percutaneous coronary intervention (PCI). Study design will take care of the real-life situation, in which patients are being offered PCI and stent placement (drug-eluting or bare metal), but also gold standard medical therapy (beta-blockers, statins, angiotensin-converting enzyme inhibitors (ACEIs), and/or calcium antagonists). Demonstrating clinical and statistical superiority of the study drug over placebo will be a real challenge. Therefore, a sequential approach has been designed with a pilot phase aiming at recruiting 50 patients. Upon evaluation of the results by an independent data steering committee, a larger sample size phase will eventually be considered.
机译:莫西度胺(一种直接的一氧化氮供体)对内皮功能障碍的影响从未使用反应性充血外周动脉眼压计 (RH-PAT) 进行评估。MEDCOR 双盲试验的目的是证明莫西多明(Coruno?16 mg,每日一次)优于安慰剂,在治疗 12 个月后改善内皮功能(RH-PAT 的 Endoscore)接受择期经皮冠状动脉介入治疗 (PCI) 的稳定型心绞痛患者。研究设计将照顾现实生活中的情况,在这种情况下,患者需要接受PCI和支架置入(药物洗脱或裸金属),以及金标准药物治疗(β受体阻滞剂、他汀类药物、血管紧张素转换酶抑制剂(ACEI)和/或钙拮抗剂)。证明研究药物相对于安慰剂的临床和统计学优势将是一个真正的挑战。因此,设计了一种顺序方法,其试点阶段旨在招募 50 名患者。在独立数据指导委员会对结果进行评估后,最终将考虑更大的样本量阶段。

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