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临床试验/NCT03587324
NCT03587324已完成不适用

Perioperative Risk Factors for the Development of Aspirin Low Response in Patients Undergoing Vascular Surgery.

St. Josef Hospital Bochum1 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2013年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
176
试验地点
1
主要终点
Number of Participants Who Were Responders or Low-Responders of Antiplatelet Therapy as a Result of Whole Blood Aggregometry Testing

研究概览

简要总结

Reduced antiplatelet activity (low response (LR)/high on-treatment platelet reactivity (HPR)) of aspirin (ALR) or clopidogrel (CLR) is associated with an increased risk of thromboembolic events. The prevalence figures for low-responders reported in the literature vary widely and there have been few investigations in vascular surgery patients to date. The aim of this prospective monocentric study was to increase the evidence base on vascular surgery patients and to detect any changes in the response following vascular surgery procedures.

详细描述

The activity of aspirin (acetylsalicylic acid, ASA) and clopidogrel is measured by whole blood impedance aggregometry using a multiple electrode aggregometer (Multiplate). The agonists used are arachidonic acid for aspirin and adenosine diphosphate (ADP) for clopidogrel. Vascular patients requiring treatment for peripheral artery disease (PAD) and/or carotid stenosis are included in the study. To identify possible risk factors demographic data, concomitant medication, laboratory parameters, co-morbidities, severity of the condition and the type of procedure performed are documented. In addition, a follow-up aggregometry is performed after completion of the vascular procedure.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Vascular patients requiring treatment for peripheral artery disease (PAD) and/or carotid stenosis are included in the study.

排除标准

  • non-adherence to the antiplatelet medication
  • abnormal platelet count in patients,
  • current gastrointestinal disorders,
  • current infections,
  • serious concomitant medical conditions (such as recent gastrointestinal bleeding, cancer, severe cardiac or liver disorders)
  • known bleeding or coagulation disorders,

研究组 & 干预措施

Experimental: aspirin, clopidogrel

Experimental

Perioperative measurement of ASA and clopidogrel resistance in patients undergoing vascular treatment

干预措施: Whole blood aggregometry before and after vascular treatment (ASA/ Clopidogrel). (Drug)

结局指标

主要结局

Number of Participants Who Were Responders or Low-Responders of Antiplatelet Therapy as a Result of Whole Blood Aggregometry Testing

时间窗: 2 years

In patients treated with aspirin and clopidogrel aggregometry was performed and depending on the results the patients were either responder or low-responder of antiplatelet therapy.

次要结局

未报告次要终点

研究者

发起方
St. Josef Hospital Bochum
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Thomas Hummel

Thomas Hummel MD, head of the arterial department, vice head of the vascular department

St. Josef Hospital Bochum

研究点 (1)

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