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临床试验/NCT02393300
NCT02393300已完成3 期

Comparison of Topical Versus Intravenous Tranexamic Acid in Primary Total Knee Arthroplasty:A Prospective Randomized Study

Shanghai Jiao Tong University School of Medicine1 个研究点 分布在 1 个国家目标入组 174 人开始时间: 2014年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
174
试验地点
1
主要终点
Total Blood Loss(TBL)

研究概览

简要总结

Previous studies in both the cardiovascular and orthopedic study have shown tranexamic acid (TXA) reduces blood loss and post-operative blood transfusion rate largely without major complications . In addition, many meta-analyses have confirmed these results . However, there is little information about comparison among the different routes of TXA administration in TKA. Therefore, this study has been designed to determine which administration route of TXA is more effective and safety.

详细描述

Objectives:To assess the efficacy and safety between the two different applying routes.

Patients in this project will be randomly divided into three groups , one group is a blank group and the rest two receive either the topical or the intravenous form of tranexamic acid during unilateral TKA(total knee arthroplasty).The total blood loss(TBL) will be calculated as the primary outcome for efficacy while Deep Vein Thrombosis、Pulmonary Embolism、Acute Myocardial Infarction 、 Acute Kidney Infarction and Cerebral Infarction events will be recorded to assess the safety of the tranexamic acid during a six-week follow-up for each patient.

All surgery are under general anesthesia, through direct lateral approach with cementless prosthesis.For all patients, the drain tube will be clamped and closed completely for 2 hours; then the clamp will be fully opened.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Consented to join in our project.
  • Adult patients (greater than 18 years old)
  • Patients scheduled for primary unilateral knee arthroplasty

排除标准

  • Patients who refuse to sign the Inform Consent
  • Had an allergy to TXA.
  • Using anticoagulant drugs within a week.
  • Coagulopathy (preoperative platelet count <150,000/mm3,International Sensitivity Index(INR)>1.4, prolonged Activated Partial Thromboplastin Time,Prothrombin Time ,or thrombin time >1.4 times longer than normal.
  • Breastfeeding
  • Major comorbidities: Severe ischemic heart disease(class III and IV of New York Heart Association); sleep apnea syndrome; renal dysfunction ( glomerular filtration rate<60); or hepatic disfunction(glutamic-pyruvic transaminase>80 or glutamic oxalacetic transaminase>80).Retinopathy (disturbances of color vision).
  • 9.History of thromboembolic disease

研究组 & 干预措施

Group1

Placebo Comparator

60 Milliliters(ml)Normal saline (0.9% sodium chloride) will be applied by soaking the knee cavity for at least 3 minutes before wound closure and then sucked away.

干预措施: normal saline (Drug)

Group2

Experimental

two-dose intravenous tranexamic acid will be applied as follow: 10mg/kg of Tranexamic Acid in 100 Milliliters(ml) normal saline (0.9% sodium chloride),the first dose 15' before the tourniquet deflation and the second dose at 180' after the first dosage

干预措施: Tranexamic Acid (Drug)

Group 3

Experimental

3g Tranexamic Acid diluted to 60 Milliliters(ml) with normal saline (0.9% sodium chloride) will be applied by soaking the knee cavity for at least 3 minutes before wound closure and then sucked away.

干预措施: Tranexamic Acid (Drug)

结局指标

主要结局

Total Blood Loss(TBL)

时间窗: calculated by an equation at the fifth postoperative day

Total Blood Loss(TBL) was calculated with equations described by Gross et al.

次要结局

  • Transfusion rates(from the day of surgery to the day of discharge,an expected average of 7 days)

研究者

发起方
Shanghai Jiao Tong University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

zhoukaidi

MD in Shanghai Jiao Tong University School of Medicine

Shanghai Jiao Tong University School of Medicine

研究点 (1)

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