NCT01409278已完成不适用
The Evaluation of the Efficacy of Local Infiltration Analgesia and Infusion for Total Hip Arthroplasty
Trinity Health Of New England2 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2009年8月1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
- 105
- 试验地点
- 2
- 主要终点
- The pain medication requirement for 48 hours after surgery in three groups.
研究概览
简要总结
The purpose of this study is to examine three different ways to control pain after hip replacement:
- One time injection of ropivacaine before wound closure
- One time injection of ropivacaine before wound closure plus slow release of ropivacaine via catheter for 48 hours
- Standard practice of patient controlled pump
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •total knee replacement
排除标准
- •History of neurological disease, diabetes, pregnancy, allergy to local anesthetic solutions chronic narcotic use ability to consent
结局指标
主要结局
The pain medication requirement for 48 hours after surgery in three groups.
时间窗: 48 hours after surgery
次要结局
- Pain scores, incidence of nausea and vomiting and patient satisfaction in each group.(48 hours after surgery)
研究者
研究点 (2)
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