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临床试验/NCT00940784
NCT00940784撤回2 期

MPD-RC 108: Phase II, Randomized, Double-Blind, Placebo Controlled International Study of Clopidogrel and Aspirin for the Treatment of Polycythemia Vera

Ronald Hoffman0 个研究点开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
撤回
发起方
主要终点
To determine the safety and efficacy of using Clopidogrel plus aspirin on Polycythemia Vera patients

研究概览

简要总结

Clopidogrel (Plavix) and aspirin are two antithrombotic agents (blood thinners) commonly used in patients with previous thrombotic events (stroke or heart attack). Thrombosis is the formation of a blood clot in a blood vessel. Patients with polycythemia vera are routinely treated with aspirin which has been shown to be effective in reducing their thrombotic risk. However, in polycythemia vera patients with previous thrombosis, a further benefit might be obtained by using the combination of aspirin and clopidogrel which is routinely used in patients with recent acute myocardial ischemia (reduced blood supply to the heart muscle). The study will assess whether this combination therapy greatly increases the risk of bleeding versus aspirin alone, if clopidogrel reduces biological factors that might lead to a stroke or heart attack, and whether a high number of patients with polycythemia vera are resistant to clopidogrel.

Approximately 200 subjects will be enrolled to the Myeloproliferative Disorders-Research Consortium (MPD-RC) study in Europe and the United States with participation expected to last for 7 months (6 months of receiving study medication plus a 30 day follow-up visit).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 81 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

Clopidogrel

Experimental

Subjects will be randomized to clopidogrel (oral-75 mg per day) in addition to low dose aspirin and hydroxyurea

干预措施: Clopidogrel (Plavix) (Drug)

Clopidogrel

Experimental

Subjects will be randomized to clopidogrel (oral-75 mg per day) in addition to low dose aspirin and hydroxyurea

干预措施: Aspirin (Drug)

Placebo

Placebo Comparator

Subjects will be randomized placebo in addition to low dose aspirin and hydroxyurea

干预措施: Placebo (Drug)

Placebo

Placebo Comparator

Subjects will be randomized placebo in addition to low dose aspirin and hydroxyurea

干预措施: Aspirin (Drug)

结局指标

主要结局

To determine the safety and efficacy of using Clopidogrel plus aspirin on Polycythemia Vera patients

时间窗: 2 years

次要结局

未报告次要终点

研究者

发起方
Ronald Hoffman
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ronald Hoffman

Professor of Medicine, Hematology and Medical Oncology

Icahn School of Medicine at Mount Sinai

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