NCT01283087已完成不适用
Spinal Anesthesia Using Lidocaine and Sufentanil and TNS (=Transient Neurological Symptoms)
Vestre Viken Ringerike Sykehus2 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2011年1月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 168
- 试验地点
- 2
- 主要终点
- Symptoms of transient neurological symptoms
研究概览
简要总结
The purpose of this study is to find out whether patients receiving spinal anesthesia containing lidocaine and sufentanil get transient neurological symptoms.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
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
- •adults over the age of seventeen years
排除标准
- •patient refuse spinal anesthesia
- •spinal anesthesia is contraindicated
- •pregnancy
- •patient is incapable of giving consent
- •neurological disorders
- •chronic pain
- •chronic use of analgesics
- •spinal anesthesia within five days before the actual surgery
结局指标
主要结局
Symptoms of transient neurological symptoms
时间窗: 5 days
次要结局
未报告次要终点
研究者
Britt-Marie Berling
MD, PhD
Vestre Viken Ringerike Sykehus
研究点 (2)
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