ACTRN12610000766011已完成未知
A study to compare the effectiveness, when applied to clinical practice of an ‘accelerated’ chest pain diagnostic pathway, against the standard investigative process for adults presenting with possible cardiac chest pain at Christchurch Hospital.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 542
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
- Randomised controlled trial
- 主要目的
- Diagnosis
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •1.Adults > 18 years of age
- •2.Presenting acutely to Christchurch hospital ED with chest pain (or discomfort) suggestive of AMI for whom, following initial clinical assessment, the attending clinician(s) intends to perform serial Cardiac Troponin (cTns), as part of the current chest pain investigation pathway for possible AMI.
排除标准
- •1. ST Segment Elevation Myocardial Infarction (STEMI) present on any ECG.
- •2. Aged less than 18 years old
- •3. Proven or suspected non-coronary pathology as the cause of chest pain
- •4. Patients who will require admission regardless of a negative cTn, due to other medical conditions, need for other investigations or social considerations.
- •5. Transfers from other hospitals
- •6. Chest pain episode began over > 12 hours ago and still persisting pain
- •7. Subjects previously enrolled in this study
- •8. Patient (or Legal Representative) unable or unwilling to provide informed consent.
- •9. Anticipated problem with follow-up e.g. resident outside New Zealand
- •10. Researcher does not feel that recruitment is appropriate (e.g. terminal illness)
研究者
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