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临床试验/IRCT2016110720258N17
IRCT2016110720258N17招募中2 期

Comparison addition morphine and Tramadol to 1.5% lidocaine with para ?cervical block in reducing of post operative pain in patient candidate curettage

Vice chancellor for research, Arak University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
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

  • age 20 to 45; ASA class I and II; block by one person; curettage by one person; duration of curettage in 20 minute.
  • Exclusion criteria: failure in general anesthesia; history of underlying disease; allergy to drug of anesthesia

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research, Arak University of Medical Sciences

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