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
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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