跳至主要内容
临床试验/NCT02148939
NCT02148939已完成不适用

Dipyrone Nullifies Aspirin Antiplatelet Effects in Stroke-Patients

Heinrich-Heine University, Duesseldorf1 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
61
试验地点
1
主要终点
Laboratory response to aspirin therapy in metamizole co-medicated Stroke patients

研究概览

简要总结

Many patients suffer from acute and chronic pain. The incidence of chronic pain correlates with increased age. Most of patients rely on analgesic medication to control the pain. Dipyrone is an extensively used drug in Western and Eastern Europe as well as Central and South America, largely due to its favorable analgesic and antipyretic effects in conjunction with a low incidence of gastrointestinal complications when compared to other non-steroidal anti-inflammatory drugs (NSAIDs).

Aspirin is the backbone of antiplatelet therapy in patients after ischemic stroke. However, it is known that there are substantial inter-individual response variabilities to antiplatelet medication. Furthermore, patients with impaired response to aspirin have a significant higher risk of recurrent cerebrovascular events. The investigators have recently shown that co-medication with aspirin and dipyrone in patients with coronary artery disease lead to insufficient antiplatelet effects of aspirin.

The incidence of chronic pain is very high in patients with ischemic stroke. Therefore, in this study the investigators aim to examine, if co-medication of aspirin and dipyrone interaction also occurs in patients after ischemic stroke.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Age ≥ 18 years
  • Patients with ischemic stroke and ASS-medication (80-320 mg/day) with/without analgesic comedication

排除标准

  • Reanimation
  • cardiogenic shock

结局指标

主要结局

Laboratory response to aspirin therapy in metamizole co-medicated Stroke patients

时间窗: Baseline

次要结局

  • Major adverse cardiac and cerebrovascular events (MACCE Events) during hospital stay(participants are followed until discharge up to 4 weeks)

研究者

发起方
Heinrich-Heine University, Duesseldorf
申办方类型
Other
责任方
Principal Investigator
主要研究者

Klinik für Kardiologie, Pneumologie und Angiologie

Division of Cardiology, Pulmonary Diseases, Vascular Medicine

Heinrich-Heine University, Duesseldorf

研究点 (1)

Loading locations...

相似试验