IRCT20190204042618N3已完成3 期
Comparing the efficacy of standard spinal anesthesia and transversus abdominis plane block with Ropivacaine 0.5% on relieving the postoperative pain after laparoscopic gynecologic surgery
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 200
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
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •Candidate for laparoscopic gynecologic surgery (such as ovarian cystectomy and hysterectomy)
- •Willingness to participate in the study
排除标准
- •Having a history of allergy to the agents used in the study
- •suffering from acute and/or chronic preoperative pains
研究者
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