IRCT201305204686N7已完成2 期
Comparision of adition of Fentanyl and Ketamin to 5/1% lidocaine with paracervical block in reducing of post operative pain in curettage
Arak University of Medival Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 120
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
- 20 years 至 45 years（—）
- 性别
- Female
入选标准
- •patient candidate curettage; age 20-45 years old; informed written consent for paracervical block.
- •Exclusion criteria: prolonged procedure >20 minutes; failure of block and need to general analgesia; allergy to analgesic substances occurring of any heart diseases.
排除标准
- 未提供
研究者
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