TCTR20150608001已完成2 期
Parenteral parecoxib provides similar analgesic efficacy to single-shot sciatic nerve block after total knee arthroplasty when combined with continuous femoral nerve block
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 78
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 0 Years 至 100 Years（—）
- 性别
- All
入选标准
- •- Adults undergoing unilateral TKA
- •- Written informed consent obtained
排除标准
- •- Infection at the planned site of skin puncture, coagulopathy, known allergy to local anesthetics, and inability to operate a patient-controlled analgesia device (PCA). Patients with relative contraindications to intravenous parecoxib, such as coronary artery disease, cerebrovascular disease, asthma and severe renal function impairment.
研究者
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