跳至主要内容
临床试验/IRCT20101211005362N31
IRCT20101211005362N31招募中1 期

Comparison study of the preemptive of the two dose of dexmedetomidine (bolus and infusion) on post operative pain, nausea and vomiting for laparoscopic cholecystectomy

Esfahan University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
90

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
18 years 至 65 years(—)
性别
All

入选标准

  • patient candidate to be operated laparoscopic cholecystectomy
  • one and two ASA
  • age between 18 - 65 year
  • Patient consent to participate in the study

排除标准

  • Drug addiction
  • History of dexmedetomidine allergy
  • People with a BMI above 30
  • Use of sleeping pills and analgesics chronically

研究者

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