ACTRN12617001546347已完成4 期
A comparison of efficacy of three techniques for regional anaesthesia in patients undergoing shoulder arthroscopy.
Orthopaedic Research Institute of Queensland0 个研究点目标入组 130 人开始时间: 2017年11月9日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 130
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 90 Years（—）
- 性别
- All
入选标准
- •Patients scheduled to undergo shoulder arthroscopy under the care of the investigating surgeons.
- •Male and female
- •Able to provide informed consent
- •Patients with BMI <40
- •Patients not currently taking regular opioid analgesics
排除标准
- •Patients with distorted anatomy that may negatively impact on block insertion
- •Patients with pre-existing nerve injury/neuropathy affecting the innervation of the upper limb & shoulder.
- •Patients with a known adverse drug reaction to the medications used in this study
- •Patients with comorbid medical conditions that would contraindicate block insertion (i.e. ISB in severe COPD)
- •Patients unable to comply with assessment requirements
- •Patients with active infection
- •Patients with BMI >40
- •Patients who are pregnant or planning on becoming pregnant during the course of the study
- •Patients unable to provide informed consent
研究者
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