JPRN-UMIN000026993已完成未知
PRediction of Opioid-induced respiratory Depression In patients monitored by capnoGraphY (PRODIGY) - PRODIGY
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 1,650
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Expected length of stay =<24 hours. 2.Patient is receiving intrathecal opioids. 3.Post-surgical patients with American Society of Anesthesiologists physical status (ASA PS) V or higher. 4.Patients with the status of Do Not Resuscitate (DNR), hospice, or receiving end of life therapy. 5.Ventilated or intubated patients. 6.Patient is unwilling or unable to comply fully with study procedures (including non-toleration of the capnography cannula) due to any disease condition which can raise doubt about compliance and influencing the study outcome. 7.Patient is a member of a vulnerable population, includinglegal incapacity or evidence that a subject cannot understand the purpose and risks of the study, regardless of authorized representative support. 8.Patient is participating in another potentially confounding drug or device clinical study.
研究者
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