EUCTR2016-000071-24-ES进行中(未招募)不适用
TIME OF ADMINISTRATION OF TRANEXAMIC ACID TO PREVENT BLEEDING IN TOTAL KNEE ARTHROPLASTY
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •-Adult patients of both genre aged between 18 and 85 years.
- •- Patients scheduled for primary and unilateral total knee arthroplasty with tourniquet.
- •- Patients who signed informed consent indicating that they have been informed of all pertinent aspects of the trial.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 32
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 160
排除标准
- •-Pregnancy or risk of pregnancy ( fertile women who do not take contraceptives) or lactating.
- •- Participation in a clinical drug research before 3 months in pre-drug administration.
- •- Congenital or acquired bleeding disorder including thrombophilia.
- •- Absolute or relative contraindications of tranexamic acid administration :
- •- venous or arterial thrombosis
- •- pulmonary thromboembolism
- •- paroxysmal atrial fibrillation
- •- chronic kidney failure with GFR <40mm
- •- epilepsy (seizures in the last year)
研究者
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