ACTRN12606000147583进行中（未招募）1 期
A prospective, randomised study to investigate if a patient-individualised dose regimen of enoxaparin reduces the incidence of bleeding and bruising as compared to conventional dosing in patients with ACS, AF, DVT and PE.
QHDAC0 个研究点目标入组 120 人开始时间: 2006年4月27日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 ot stated（—）
- 性别
- All
入选标准
- •Any patient (male or female) initiated or about to be initiated on treatment doses of enoxaparin.
排除标准
- •Pregnancy, anticoagulation in the past 7 days, abnormal liver function test (more than twice the usual range).
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