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
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.
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