跳至主要内容
临床试验/NCT02227368
NCT02227368终止2 期

A Phase II Multicentre, Randomised, Double-Blind, Controlled, Parallel-Group Study to Evaluate the Walking Time Effect of Long-Term Ticagrelor in Comparison to Long-Term Aspirin Administration in Ambulatory Patients With Peripheral Artery Disease Undergoing Endovascular Revascularization - The Ticagrelor in Peripheral Artery Disease Endovascular Revascularization Study TI-PAD I EVR

AstraZeneca1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年10月20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
终止
发起方
AstraZeneca
入组人数
40
试验地点
1
主要终点
Change From Baseline in Log Transformed Peak Walking Time (PWT) at Week 26 or Early Termination (ET)

研究概览

简要总结

To compare the effect of ticagrelor versus aspirin on the change in peak walking time, evaluated on the graded treadmill test, from one to 26 weeks post-revascularization in patients with peripheral artery disease who have undergone endovascular revascularization for moderate to severe claudication or ischemic rest pain.

详细描述

A Phase II Multicentre, Randomised, Double-Blind, Controlled, Parallel-Group Study to Evaluate the Walking Time Effect of Long-Term Ticagrelor in Comparison to Long-Term Aspirin Administration in Ambulatory Patients with Peripheral Artery Disease Undergoing Endovascular Revascularization - The Ticagrelor in Peripheral Artery Disease Endovascular Revascularization Study TI-PAD I EVR.

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
50 Years 至 130 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

Ticagrelor

Experimental

26 Weeks of ticagrelor 90mg twice a day plus aspirin placebo once daily

干预措施: Ticagrelor (Drug)

Aspirin

Active Comparator

26 Weeks of aspirin 100mg once daily plus ticagrelor placebo twice a day

干预措施: Comparator (Drug)

结局指标

主要结局

Change From Baseline in Log Transformed Peak Walking Time (PWT) at Week 26 or Early Termination (ET)

时间窗: 26 Weeks

次要结局

  • Change From Baseline in Log Transformed Claudication Onset Time (COT) at Week 26 or Early Termination (ET)(26 Weeks)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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