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临床试验/IRCT20161126031095N4
IRCT20161126031095N4招募中2 期

Comparison of the effect of adding dexmedetomidine with dexamethasone to bupivacaine in abdominal transverse block on pain intensity after laparoscopic cholecystectomy

Mazandaran University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
100

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

  • ASA class I and II physical condition
  • Age between 18-65 years

排除标准

  • Patient refusal to participate
  • Neuromuscular diseases (eg myopathy, myasthenia gravis)
  • Hematological diseases, bleeding or coagulation disorders
  • Local skin infection and sepsis at the block site
  • Known hypersensitivity to study drugs
  • Morbid obesity (BMI > -35.7
  • History of alcoholism or drug addiction
  • Any uncompensated systemic disease (cardiovascular, respiratory, metabolic, neurological and endocrine)
  • Other mental or emotional problems that may invalidate informed consent. Patients will be screened by a preoperative care nurse. Potentially eligible individuals will be directed to investigators for screening and additional information.
  • Sleep apnea or any other sleep disorder

研究者

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