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临床试验/CTRI/2017/07/009076
CTRI/2017/07/009076已完成未知

The comparative Efficacy and Safety of Topical and Intravenous Tranexamic acid for Reducing Perioperative Blood Loss in Total Knee Arthroplasty- A Randomized Controlled Non-inferiority Trial

SUNSHINE HOSPITALS0 个研究点目标入组 113 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
113

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. All patients undergoing total knee arthroplasty for primary
  • arthroplasty knee
  • 2.Patients who are willing to participate in the study.
  • 3.Patient without exclusion criteria.

排除标准

  • 1.Allergy to the TXA
  • 2.H/O Coagulopathy,abnormal PT or APTT
  • 3.Past H/O Thromboembolic event
  • 4.Treatment with Aspirin or NSAIDS in the last week
  • 5.plasma creatinine > 115 micro moles /litre for males
  • And >100 micro moles/litre in females.
  • 6.Acute infection[eg;leukocytosis or fever]
  • 7.Malignancy
  • 8.MI in preceding 12 months,unstable angina
  • 9.Patient who were given plasma in perioperative period

研究者

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