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临床试验/EUCTR2016-000071-24-ES
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

Consorci Mar Parc de Salut de Barcelona (Parc de Salut MAR)0 个研究点开始时间: 2016年2月3日最近更新:
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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