ACTRN12611001166965招募中4 期
Comparison of dexamethasone route of administration on ankle block duration and analgesia for foot and ankle surgery
Ms Rachel Dawson0 个研究点目标入组 90 人开始时间: 2011年11月8日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 90
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 o limit（—）
- 性别
- All
入选标准
- •Elective patients having metatarsal osteotomy for foot surgery
- •American Society of Anaesthesiologists score 1-3
排除标准
- •American Society of Anaesthesiologists score of 4 or greater
- •Contraindication to ankle block (patient refusal, coagulopathy, sepsis, local infection, allergy to ropivacaine)
- •Contraindication to dexamethasone (eg. known hypersensitivity, poorly controlled diabetes mellitus)
- •Pre-existing sensory deficit around the site of surgical intervention (eg. peripheral neuropathy, stroke)
- •Systemic glucocorticoid treatment of >10mg prednisolone (or equivalent) for two weeks or more within three months of surgery
- •Chronic opioid use define as >30mg oral morphine per day or equivalent (Fentanyl patch 12mcg/hr; buprenorphine 20mcg/hr; oxycodone >20mg/day)
- •Contraindication to non-steroidal anti-inflammatory drugs (NSAIDs) (eg. known hypersensitivity, active peptic ulcer disease, renal impairment, pregnancy)
- •Previous enrolment in this study
- •Inability to understand english
研究者
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