Prospective Randomized On-X Anticoagulation Clinical Trial (PROACT)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 977
- 试验地点
- 96
- 主要终点
- Bleeding Events
研究概览
简要总结
Various patient groups with the On-X Valve can be maintained safely on lower doses of blood thinner(Coumadin®) or on antiplatelet drugs (aspirin/Plavix®) only rather than the standard dose of Coumadin and aspirin presently recommended by ACC/AHA or ACCP professional societies.
详细描述
This is a longitudinal, randomized (randomization to occur at the 3-month follow-up) study comparing the On-X valve on low dose anticoagulation (test group) to concomitant control groups of On-X valves receiving standard Coumadin/aspirin therapy, and also to FDA objective performance criteria (OPC) for heart valve replacement. It is a multicenter study consisting of up to 50 centers in the United States, Canada, and Italy enrolling and randomizing no more than 1200 patients (200 in each of 6 groups). There are three test arms of the study: low risk aortic valve replacement, high risk aortic valve replacement, and mitral valve replacement. Each arm has an equivalent control. Test therapies are: low risk aortic valve replacement - aspirin/Plavix, high risk aortic valve replacement - Coumadin at INR of 1.5 to 2.0 plus aspirin, and mitral valve replacement - Coumadin at an INR of 2.0 to 2.5 plus aspirin. Follow-up will run for up to 8 years in each patient. Each arm is independent and the low risk aortic and high risk aortic arms are completed. The low risk aortic arm was closed early resulting in a reduction of the estimated total enrollment with randomization to 1000. The high risk arm is completed with FDA review and this arm had 375 randomized enrollees. The mitral arm continues to enroll with a planned randomized enrollment of 400.
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
- None
盲法说明
Number of participants below refers to randomized in all 3 study arms
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients requiring isolated aortic valve replacement (AVR), or isolated mitral valve replacement (MVR).
- •AVR patients receiving low dose or antiplatelet only anticoagulation will be divided into groups at low risk and high risk for thromboembolism with all patients being in the low risk group except for patients with the following conditions which place a patient in the high risk group:
- •Chronic atrial fibrillation
- •Left ventricular ejection fraction < 30 %
- •Enlarged left atrium >50mm diameter
- •Spontaneous echo contrasts in the left atrium
- •Vascular pathology
- •Neurological events
- •Hypercoagulability
- •Left or right ventricular aneurysm
- •Lack of platelet response to aspirin or clopidogrel
- •Women receiving estrogen replacement therapy
- •Concomitant cardiac surgery is allowed
- •Adult patients
排除标准
- •Right side valve replacement
- •Double (aortic plus mitral) valve replacement
- •Patients with active endocarditis at the time of implant
- •Previous confirmed or suspected thromboembolic event or thrombophlebitis
- •Other terminal illness
- •Patients who are in an emergency state
- •Inability to return for required follow-ups
- •Patients with an On-X valve implanted within the study and subsequently explanted
- •Patients who are known to be pregnant, plan to become pregnant or are lactating
- •Patients with acquired immunodeficiency syndrome or know to be HIV positive
- •Patients who are prison inmates or known drug or alcohol abusers
- •Patients unable to give adequate informed consent.
结局指标
主要结局
Bleeding Events
时间窗: 8 years
Percentage of events per patient year
Thromboembolism
时间窗: 8 years
Percentage of events per patient year
Valve Thrombosis
时间窗: 8 years
Percentage of events per patient year
次要结局
- Valve-Related Mortality(8 years)
- Valve Hemodynamics(5 years)