跳至主要内容
临床试验/CTRI/2013/08/003931
CTRI/2013/08/003931进行中(未招募)未知

ong-Term rIsk, clinical management and healthcare Resource utilization of stable coronary artery diSease in post myocardial infarction patients. - TIGRIS

AstraZeneca AB0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
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
Observational

入排标准

入选标准

  • The subject population that will be observed in the NIS must fulfil all of the following criteria:
  • Provision of subject informed consent
  • Female and/or male aged 50 years and over
  • Documented history of presumed spontaneous MI (excluding known peri-procedural or definite secondary MI [eg, due to profound hypotension, hypertensive emergency, tachycardia, or profound anemia]) with their most recent MI occurring 1 to 3 years prior to enrollment and have at least 1 of the following risk factors:
  • Age . 65 years
  • . Diabetes mellitus requiring medication
  • . Documented history of a second prior presumed spontaneous MI ( >1 year ago)
  • . Documented history of angiographic evidence of multivessel coronary artery disease (CAD)
  • . Chronic, non-end stage renal dysfunction (15 mL/min . creatinine clearance, calculated by Cockcroft Gault equation, <60 mL/min)

排除标准

  • Patients will not be eligible to participate if any of the following exclusion criteria are present:
  • Presence of any condition/circumstance which in the opinion of the investigator could significantly limit the complete follow up of the patient (e.g. tourist, non-native speaker or does not understand the local language where interpreter services are not reliably available, psychiatric disturbances, alcohol or drug abuse).
  • Presence of serious/severe co-morbidities in the opinion of the investigator which may limit life expectancy ( <1 year).
  • Current participation in a blinded randomized clinical trial.
  • Patients receiving treatment of ticagrelor beyond 12 months or off label use of ticagrelor.

研究者

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