跳至主要内容
临床试验/DRKS00000132
DRKS00000132招募中4 期

Randomized, Double-Blind, Placebo-Controlled Trial of 6 Months versus 12 Months Clopidogrel Therapy After Implantation Of A Drug-Eluting Stent Intracoronary Stenting and Antithrombotic Regimen:Safety And Efficacy of Six-Months Dual Antiplatelet Therapy After Drug-Eluting Stenting - ISAR-SAFE

Klinik für Herz-und KreislauferkrankungenDeutsches Herzzentrum München0 个研究点目标入组 6,000 人开始时间: 2009年6月17日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
6,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
19 Years 至 one(—)
性别
All

入选标准

  • 1. Patients on clopidogrel therapy at 6 months (- 1/+2 months) after DES implantation
  • 2. Informed, written consent by the patient

排除标准

  • 1. Age =18 years
  • 2. Clinically symptoms, signs of ischemia and/or presence of angiographic lesions requiring revascularization
  • 3. Previous stent thrombosis
  • 4. DES in left main coronary artery
  • 5. ST-elevation and non ST-elevation myocardial infarction during the last 6 months after DES implantation
  • 6. Malignancies or other comorbid conditions with a life expectancy of less than one year or that may result in protocol noncompliance
  • 7. Planned major surgery within the next 6 months with the need to discontinue antiplatelet therapy
  • 8. Active bleeding; bleeding diathesis; history intracranial bleeding
  • 9. Oral anticoagulation therapy with coumarin derivatives
  • 10. Known allergy or intolerance to the study medications: aspirin and clopidogrel
  • 11. Pregnancy (present, suspected or planned) or positive pregnancy test
  • 12. Patient's inability to fully comply with the study protocol
  • 13. Enrollment in another clinical trial before reaching the primary endpoint

研究者

发起方
Klinik für Herz-und KreislauferkrankungenDeutsches Herzzentrum München

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