NL-OMON51650招募中不适用
RCT to assess In hospital 24 hour observation with telemetry of Syncope patients admitted to the Cardiac Emergency Room - SYNCOPE R.I.S.C. trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 640
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
- 年龄范围
- 18 至 99（—）
入选标准
- •All patients with low risk- and intermediar risk syncope presented on the
- •Cardiac Emergency Care, will be eligible for the study.
排除标准
- •(1) Those aged <18 years
- •(2) Those in whom syncope / transient loss of consciousness co-exisits with
- •trauma or other serious condition identified in the CER (massive bleeding,
- •pulmonary embolus) or any high-risk features upon assessment with guideline
- •based SA (see appendix 2)
- •(3) Those with any other conditions then syncope / transient loss of
- •consciousness for which admission is required (including social indication for
- •admission, etc.)
- •(4) Contraindication for early discharge at the discretion of the responsible
- •(5) Those with a learning disability
- •(6) Those presenting with pre-syncope
- •(7) Those who are unwilling to provide informed consent (those will be asked to
- •be enrolled for the SYNCOPE R.I.S.C - registry)
研究者
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