NCT01362075终止不适用
Pain Management After Shoulder Arthroplasty: A Randomised Clinical Trial of Interscalene Block and Local Infiltration Analgesia
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 74
- 试验地点
- 4
- 主要终点
- Supplemental analgesics ingested
研究概览
简要总结
The purpose of this study is to determine the efficacy of local infiltration analgesia as compared to 48-hour interscalene block in treating pain after shoulder arthroplasty. The investigators hypothesize a reduced pain score and use of supplemental analgesic medication during the first three postoperative days using local infiltration analgesia.
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
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •elective primary shoulder arthroplasty
排除标准
- •reverse or delta prosthesis
- •recent fracture near the shoulder
- •allergic to amid-type local analgesics
- •operation not under general anaesthesia
- •incompetent, pregnant, below 18 or above 90 years old
- •severe chronic neurogenic pain or sensory disturbances in the shoulder
结局指标
主要结局
Supplemental analgesics ingested
时间窗: First 24 hours postoperatively
次要结局
- Pain score(First 72 hours postoperatively)
- Supplemental analgesics ingested(First 72 hours postoperatively)
研究者
Karen Toftdahl Bjørnholdt
MD
Horsens Hospital
研究点 (4)
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