ACTRN12611000206921已完成未知
Rapid assessment of cardiac chest pain: A prospective validation trial.
Investigator initiated study - Dr Louise Cullen, Senior Staff Specialist0 个研究点目标入组 1,000 人开始时间: 2011年2月22日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,000
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
- Non-randomised trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patient with symptoms of greater than or equal to 5 minutes consistent with possible ACS (chest discomfort or angina equivalent)
- •Physician plans to evaluate the patient for potential ACS
- •Intermediate risk features on QLD CPP
排除标准
- •More than 2 hours since arrival at hopsital.
- •Patient (or Legal Representative) is unable or unwilling to provide informed consent.
- •Transfer from other hosptial.
- •Patient (or Legal Representative) refusal of telephone follow-up or medical record review at 30 days or unlikely to be contactable for follow-up.
- •Reasearcher does not feel that informed consent is obtainable or that recruitment is apporpriate (e.g. terminal illness).
- •Clear alternative non-ACS diagnostic cause for symptoms.
- •High risk features according to QLD CPP.
研究者
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