KCT0001202已完成未知
Postoperative intravenous patient controlled analgesic efficacy of nefopam after laparoscopic gynecologic surgery
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 21(Year) 至 76(Year)(—)
- 性别
- Female
入选标准
- •American Society of Anesthesiologist (ASA) physical status I–II patients scheduled to undergo laparoscopic gynecologic surgery
排除标准
- •Patients with preexisting neurological deficit, renal and hepatic dysfunction, obese (BMI > 30 kg/m2), drug abuse or hypersensitivity to drugs, pregnancy
研究者
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