NL-OMON48393已完成不适用
Comparison of peripheral venous and arterial blood gas in management of patients with respiratory complaints in the emergency department. - Blood Gas Comparison trial (BGC trial)
Zuyderland Medisch Centrum0 个研究点目标入组 155 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 155
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
- •Patients (* 18 years) presenting in the ED with dyspnoea, respiratory rate >
- •20/min or peripheral oxygen saturation < 95%, a reliable saturation measured by
- •pulse oximetry (measured with the Philips IntelliVue MP30 patient monitor, a
- •reliable measurement is defined by pulsatile flow with a perfusion indicator
- •value above 0.3) and an indication, determined by the treating physician, to
- •determine the acid-base, ventilation and oxygenation status by arterial blood
排除标准
- •A potential subject who meets any of the following criteria will be excluded
- •from participation in this study:
- •- Not capable to give informed consent within reasonable time after
- •stabilisation and abating of the accompanying psychological stress, and no
- •representative available to give informed consent on behalf of the patient.
- •- Arterial blood gas results are required for other reasons than determining
- •the acid-base, ventilation and oxygenation status, such as determining the
- •alveolar to arterial oxygen gradient (A-a gradient).
- •- No physician or qualified nurse available for ABG sampling.
- •- Failed ABG or VBG sampling after two attempts.
- •- Previous participation in the study.
研究者
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