EUCTR2013-003169-33-DK进行中（未招募）不适用
Evaluation of intra articular Tranexamic acid for reduction of total blood loss in total knee unilateral 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
- •=18 years.
- •Undergoing surgery for unilateral total knee prothesis.
- •Give one's consent.
- •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 20
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 40
排除标准
- •Allergic to TXA.
- •In treatment with the following antikoagulantia: ADP receptorinhibitors, Vitamin K antagonist (within 5 to 7 days before the operation.). Faktor Xa inhibitors, trombine-inhibitors.
- •Use og oral antikonceptiva
- •Known with Trombofili.
- •Reduced kidney function (S-kreatinine > 120 micromol/L)
- •Participated in a clinical trial within the last 30 days.
- •Alcoholisme and morphinism.
- •Females: Menstruation within the last 12 months.
- •Patients who are not able to speak and under stand Danish.
- •Patients who refuse to receive blood products.
- •Present acute thromboembolic event (DVT, AMI, lung embolia, cerebral infarction, pulmonary embolism)
- •Disseminated intravascular coagulation (DIC) or active thromoembolic disease.
- •Present active cancer disease.
研究者
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