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临床试验/NCT07268586
NCT07268586已完成4 期

Intravenous Atropine in Reducing Reperfusion Arrhythmias, Conduction Abnormalities and Hypotension in Inferior ST-elevation Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention

Ain Shams University1 个研究点 分布在 1 个国家目标入组 158 人开始时间: 2025年8月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
入组人数
158
试验地点
1
主要终点
Conduction abnormalities

研究概览

简要总结

People with acute inferior wall myocardial infarction will be given an intravenous drug called atropine that increases the heart rate to check if it prevents heart rhythm disturbances during performing coronary intervention

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Acute inferior ST elevation myocardial infarction

排除标准

  • Execution of rescur percutaneous coronary intervention after thrombolysis
  • Mechanical complications or no reflow or spontaneous reperfusion.
  • Prior implantation of permanent or temporary pacemakers
  • History of bradycardia, hypotension or ventricular tachycardia with a definitive cause (unrelated to the disease under study)
  • Prior coronary artery bypass graft surgery
  • Atropine contraindications Unwillingness to participate in the

研究组 & 干预措施

Atropine arm

Active Comparator

This group will receive intravenous atropine 1 mg immediately before wire crossing

干预措施: Intravenous atropine immediately before wire crossing during primary percutaneous coronary intervention (Drug)

Placebo arm

Placebo Comparator

This group will receive intravenous normal saline immediately before wire crossing

干预措施: Intravenous normal saline as placebo immediately before wire crossing during primary percutaneous coronary intervention (Drug)

结局指标

主要结局

Conduction abnormalities

时间窗: Periprocedurally

Occurrence of conduction abnormalities

Reperfusion arrhythmias

时间窗: Periprocedurally

Occurrence of reperfusion arrhythmias

次要结局

  • Major adverse cardiac events(Periprocedurally)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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