NCT01216488已完成3 期
Comparison of Axillary Block Under Ultrasound With 40 or 25 ml of Xylocaine 1.5% Adrenalin in Forearm or Arm Surgery.
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 72
- 试验地点
- 1
- 主要终点
- Axillary block efficiency conducted by ultrasound
研究概览
简要总结
Hospitalized patients for superior member surgery have different types of anesthesia.Forearm and/or arm surgery could be done under general anesthesia, but in the most of the cases, this surgery was done under locoregional anesthesia.Several injections of local anesthesia at the nerves axilla are used with the used of ultrasonography.
The purpose of this study is to show that the anesthesia efficiency is the same with 40 or 25 ml of Xylocaine 1.5% Adrenalin in Forearm or Arm Surgery.
详细描述
Inclusion criteria :
- age > 18 years old
- patient who must have a non emergency surgery of the forearm or the hand
- ASA I or ASA II
- informed consent
- Ensured patient
Exclusion criteria :
- pregnancy
- respiratory insufficiency
- cardiac insufficiency
- hepatic insufficiency
- renal insufficiency
- ASA III or IV
- contraindications to the locoregional anesthesia
- contraindications to the xylocaine used
- patient participate to an another clinical study
- guardianship patient
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
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
- •age > 18 years old
- •patient who must have a non emergency surgery of the forearm or the hand
- •ASA I or ASA II
- •informed consent
- •Ensured patient
排除标准
- •pregnancy
- •respiratory insufficiency
- •cardiac insufficiency
- •hepatic insufficiency
- •renal insufficiency
- •ASA III or IV
- •contraindications to the locoregional anesthesia
- •contraindications to the xylocaine used
- •patient participate to an another clinical study
- •guardianship patient
研究组 & 干预措施
40 ml of Xylocaine
Active Comparator
干预措施: Xylocaine (Drug)
25 ml of Xylocaine
Experimental
干预措施: Xylocaine (Drug)
结局指标
主要结局
Axillary block efficiency conducted by ultrasound
时间窗: 48 hours
during the hospitalisation
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
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