临床试验/NCT02961933

NCT02961933Unknown不适用

Utah Study Evaluating Apneic Oxygenation for Emergency Department Intubation

Intermountain Health Care, Inc.2 个研究点分布在 1 个国家目标入组 500 人开始时间: 2016年12月最近更新: 2020年2月11日

适应症

试验速览

阶段: 不适用
发起方: Intermountain Health Care, Inc.
入组人数: 500
试验地点: 2
主要终点: First pass success without hypoxemia

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study will determine rates of first pass success without hypoxemia in emergency department intubations with and without the use of apneic oxygenation by nasal cannula.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Supportive Care
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Patients requiring emergent Rapid Sequence or Delayed Sequence endotracheal intubation with administration of a neuromuscular blocker (Succinylcholine, Rocuronium)

排除标准

•Known prisoners
•Patients in cardiac arrest
•Patients who are intubated without the use of neuromuscular blockade (i.e., cardiac arrest, awake intubation).

结局指标

主要结局

First pass success without hypoxemia

时间窗: 10 minutes

次要结局

Change in peri-intubation saturation(0, 30, 60 and 120 seconds)
Saturation at time of tube placement(10 minutes)
Time to desaturation <93%(measured time until saturations drop below 93% during the peri-intubation period, up to 10 minutes)
Saturation at post intubation(0, 30, 60, and 120 seconds)

研究者

发起方

Intermountain Health Care, Inc.

申办方类型

Other

责任方

Sponsor

研究点 (2)

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