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临床试验/IRCT201102081138N7
IRCT201102081138N7已完成2 期

Comparison of surgical condition and bleeding during propofol or isofluran anesthesia for endoscopic sinus injury

Guilan University of Medical Sciences, Vice Chancellor for Research0 个研究点目标入组 44 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
44

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
15 years 至 45 years(—)
性别
All

入选标准

  • Patients candidated for elective endoscopic sinus surgery (15-45yr); ASA class I,II; Patients with completely treated nose and sinus infections
  • Exclusion criteria:
  • History of hemorrhagic disease; Seizure; Drugs that affect on the surgical homeostasis; Anemia (Hb <10); Poor controlled cerebrovascular accident; History of significant CAD; Arrhythmia; Liver or kidney dysfunction; Electrolyte or metabolic abnormalities; COPD; Severe asthma or other severe respiratory disease; History of PUD; Pregnancy

排除标准

  • 未提供

研究者

发起方
Guilan University of Medical Sciences, Vice Chancellor for Research

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