NCT03331237Unknown不适用
Shoulder Analgesia Sparing Diaphragm; ISO Block Versus Low Volume Scalene Block. A Randomized Controlled Double Blind Study
Healthpoint Hospital2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2017年10月9日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 72
- 试验地点
- 2
- 主要终点
- hemi-diaphragmatic pariesis
研究概览
简要总结
For shoulder analgesia, both ISO block and low volume scalene (LVS) block (using 5 ml of local anesthetics) are suggested to have a low incidence of hemi-diaphragmatic pariesis (HDP).
The aim of this study was to compare the incidence of HDP and the analgesic efficacy of the LVS block versus ISO block.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, 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
- •patients who were scheduled for arthroscopic shoulder surgery
排除标准
- •aged <18y
- •BMI >35,
- •ASA greater >III,
- •an infection at the injection site
- •has a contraindication for laryngeal mask or the medications used in this study.
研究组 & 干预措施
LVS group
Active Comparator
interscalene injection
干预措施: scalene block (Procedure)
ISO group
Active Comparator
in this group all patients will receive ISO block.
干预措施: ISO block (Procedure)
结局指标
主要结局
hemi-diaphragmatic pariesis
时间窗: 2-4 hours
diaphragmatic caudal displacement will be measured (in cm) with real time ultrasound before the block performance and after the procedure
次要结局
- duration of analgesia(24 hours)
- total morphine dose(24 hours)
- patient satisfaction(24 hours)
- analgesic efficacy (block success)(2-4 hours)
研究者
Ahmad Muhammad Taha
Consultant of aneathesia
Healthpoint Hospital
研究点 (2)
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