ACTRN12606000195550已完成不适用
A study of the efficacy of the addition of a ropivacaine infusion to the analgesia provided by pre-emptive ropivacaine and intra-operative parecoxib for reduction of peri-operative pain in adults undergoing elective arthroscopic rotator cuff surgery: a randomised double blind placebo controlled trial.
Monash University, Jennifer Coghlan PhD Scholar, Supervisors, A/Prof. Rachelle Buchbinder and A/Prof. Andrew Forbes.0 个研究点目标入组 158 人开始时间: 2006年5月24日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 158
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
- •Requiring rotator cuff surgery either subacromial decompression or tendon repair.
排除标准
- •Previous surgery to that shoulderFractures or tumoursIrreparable tendon tears.
研究者
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