NCT04695522Unknown1 期
Phase I Trial of ADR-002K for Patients With Ischemic Cardiomyopathy Who Undergo Coronary Artery Bypass Surgery
适应症
试验速览
- 阶段
- 1 期
- 入组人数
- 6
- 试验地点
- 2
- 主要终点
- Number of complication associated with drug administration method
研究概览
简要总结
Ischemic cardiomyopathy undergoing coronary artery bypass surgery
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who are clinically diagnosed with ischemic cardiomyopathy and receive CABG
- •Patients with a left ventricular ejection fraction of 40% or less by cardiac ultrasonography within 4 weeks before obtaining consent
排除标准
- •Patients who have a combination of cardiovascular disease such as severe organic valvular disease or aortic aneurysm determined by investigator or co-investigator to affect clinical trial procedure
- •Patients whose participation in a clinical trial is considered inappropriate at the discretion of the investigator or co-investigator
结局指标
主要结局
Number of complication associated with drug administration method
时间窗: 26 weeks
Feasibility of drug administration method
Amount of change in late gadolinium contrast-enhanced area at the time of screening and 6 months after surgery
时间窗: 26 weeks
Efficacy (Exploratory)
Number of participants with Adverse event
时间窗: 26 weeks
Safety assessment related to adverse events and this product
次要结局
未报告次要终点
研究者
Daisuke Mori
Assistant professor
Osaka University
研究点 (2)
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