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临床试验/IRCT20230208057358N2
IRCT20230208057358N2招募中Unknown

Comparison of total intravenous anesthesia(TIVA) with propofol and inhalation anesthesia with isoflurane in patients undergoing posterior lumbar fusion surgery: a randomized clinical trial

Hamedan University of Medical Sciences0 个研究点目标入组 66 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
入组人数
66

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

  • Candidate patients for posterior fusion surgery of lumbar vertebrae with pedicle screw fixation method
  • Patients who will have only 3 to 5 levels of lumbar spine fusion
  • Willingness and consent to participate in the study
  • Age between 18 and 65 years
  • American Society of Anesthesiologists (ASA) Class I-II physical status
  • Body mass index (BMI) less than 35 kg/m2

排除标准

  • Trauma patients
  • Allergy to anesthetics used in the study
  • Patients with severe chronic diseases (cardiovascular, respiratory, nervous, liver, kidney, electrolyte disorders)
  • patient with uncontrolled blood pressure
  • History of drug use
  • Patients who receive medication or liquid therapy outside of routine before, during and after surgery
  • History of bleeding disorders and treatment with anticoagulants
  • Excessive bleeding (more than MABL)
  • Women if they are menstruating
  • Abnormal coagulation profile (platelet count less than 50x103/µL, PTT greater than 50 seconds, or INR greater than 1.3 on preoperative testing)
  • Patients with a history of frequent nausea and vomiting and taking antiemetics in the 24 hours before surgery
  • Patients with mental disorders and mental retardation, dementia or schizophrenia
  • Recent brain surgery or cerebrovascular accidents

研究者

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