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临床试验/NCT01950299
NCT01950299已完成2 期

Interleukin-1 Blockade With Anakinra in Patients With ST-segment Elevation Myocardial Infarction - the Virginia Commonwealth University Anakinra Remodeling Trial 3

Virginia Commonwealth University2 个研究点 分布在 1 个国家目标入组 99 人开始时间: 2014年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
99
试验地点
2
主要终点
Acute Phase Response (CRP Levels)

研究概览

简要总结

VCU-ART3 is a double-blind randomized clinical trial of anakinra high dose vs anakinra standard dose vs placebo in patients with ST-segment elevation myocardial infarction (STEMI) measuring the effects on the acute rise and fall of the plasma C reactive protein levels during the first 14 days.

详细描述

VCU-ART3 is a double-blind randomized clinical trial of anakinra high dose vs anakinra standard dose vs placebo in patients with ST-segment elevation myocardial infarction (STEMI) measuring the effects on the acute rise and fall of the plasma C reactive protein levels during the first 14 days

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
21 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Anakinra (standard dose)

Experimental

Anakinra 100 mg daily for 14 days

干预措施: Anakinra 100 mg (Drug)

Anakinra (standard dose)

Experimental

Anakinra 100 mg daily for 14 days

干预措施: Placebo (Drug)

Anakinra (high dose)

Experimental

Anakinra 100 mg twice daily for 14 days

干预措施: Anakinra 100 mg (Drug)

Placebo

Placebo Comparator

Placebo for 14 days

干预措施: Placebo (Drug)

结局指标

主要结局

Acute Phase Response (CRP Levels)

时间窗: 14 days

Comparison of area-under-the-curve for CRP up to day 14

次要结局

  • Left Ventricular Ejection Fraction(12 months)
  • Left Ventricular End-systolic Volume(12 months)
  • Heart Failure(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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