NCT05695183已完成不适用
Functionality of the IV SafeLock Device in Emergency Department Setting
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Functionality of the IV SafeLock
研究概览
简要总结
The purpose of this research study is to evaluate the functionality of the IV SafeLock in the clinical emergency department setting.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Device Feasibility
- 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
- 是
入选标准
- •Emergency Department nurses who are consenting and willing to perform tasks.
- •Their patient population will include stable patients 18 or over, who present through triage, are medically stable, are able to verbally consent and require intravenous access.
排除标准
- •Emergency Department nurses who are unwilling to consent to use IV SafeLock on their patient population.
- •The patient population will exclude pregnant patients, children, prisoners, patients with dementia, or any member of protected class as specified by IRB.
- •The patients must be medically stable and not include patients presenting with acute stroke, acute myocardial infarction, severe sepsis or shock.
结局指标
主要结局
Functionality of the IV SafeLock
时间窗: Baseline
Measured on a likert scale for nurse evaluation of IV SafeLock
次要结局
未报告次要终点
研究者
Kara J. Bragg
Principal Investigator
Mayo Clinic
研究点 (2)
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