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临床试验/NCT05247385
NCT05247385已完成4 期

Platelet Aggregation and Adenosine Levels Among Patients With Stable Chronic Coronary Artery Disease Taking Ticagrelor or Prasugrel

University of Sao Paulo1 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2017年3月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
87
试验地点
1
主要终点
To compare platelet inhibition between the two groups (ticagrelor and prasugrel)

研究概览

简要总结

Prospective, single-center, double blind, double dummy, randomized trial. Platelet function tests and adenosine levels were assessed at baseline and 15 days after taking Ticagrelor with Prasugrel placebo or Prasugrel with Ticagrelor placebo in stable patients with coronary artery disease

详细描述

This was a prospective, double blinded, randomized trial that compared platelet inhibition and adenosine levels with ticagrelor (180mg loading dose, followed by 90 mg BID) versus prasugrel (60mg loading dose, followed by 10 mg QD) .

Patients were eligible if they were between 18 and 75 years old, were on aspirin without P2Y12 inhibitor at baseline and > 1 year after documented ACS. Platelet aggregation was compared with the Multiplate ADP® assay, performed at baseline and after 15 days on study medication. Adenosine plasma levels were measured with high performance liquid chromatography at the same time points

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • between 18 and 75 years old
  • were on aspirin
  • without P2Y12 inhibitor at baseline
  • > 1 year after documented acute coronary syndrome

排除标准

  • use of oral anticoagulation or P2Y12 at baseline
  • Weight < 60kg
  • History of tia or stroke
  • Any coagulation disorders
  • Refuse to sign the written consent

研究组 & 干预措施

Prasugrel group

Active Comparator

Prasugrel (60mg loading dose, followed by 10 mg QD for 15 days)

  • Ticagrelor placebo (Placebo loading dose followed by two pills a day)

干预措施: Prasugrel (Drug)

Prasugrel group

Active Comparator

Prasugrel (60mg loading dose, followed by 10 mg QD for 15 days)

  • Ticagrelor placebo (Placebo loading dose followed by two pills a day)

干预措施: Ticagrelor (Drug)

Ticagrelor group

Active Comparator

Ticagrelor (180mg loading dose, followed by 90 mg BID)

  • Prasugrel placebo (Placebo loading dose followed by one pill a day)

干预措施: Prasugrel (Drug)

Ticagrelor group

Active Comparator

Ticagrelor (180mg loading dose, followed by 90 mg BID)

  • Prasugrel placebo (Placebo loading dose followed by one pill a day)

干预措施: Ticagrelor (Drug)

结局指标

主要结局

To compare platelet inhibition between the two groups (ticagrelor and prasugrel)

时间窗: 15 days

Platelet aggregation was compared with the Multiplate ADP® assay at baseline and after 15 days on study medication

To compare adenosine levels between the two groups (ticagrelor and prasugrel)

时间窗: 15 days

Adenosine plasma levels were measured at baseline and after 15 days with high performance liquid chromatography at the same time points

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jose Carlos Nicolau

Director Coronary Care Unit

University of Sao Paulo

研究点 (1)

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