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临床试验/TCTR20211120003
TCTR20211120003Unknown3 期

The difference of extubation time after target-controlled infusion of propofol anesthesia in pediatric patients undergoing long-duration surgery among age groups

Faculty of Medicine Siriraj Hospital, Mahidol University0 个研究点目标入组 52 人开始时间: 2021年11月20日最近更新:
适应症

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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
1 Years 至 15 Years(—)
性别
All

入选标准

  • 1.Children aged 1 to 15 years old, 2.Patients with ASA physical status 1 - 3, 3.Patients who schedule for elective surgery with mild to moderate pain for more than or equal to 120 minutes duration, 4.Patients who require general anesthesia with an endotracheal tube and muscle relaxant and expected to extubate after the anesthesia

排除标准

  • 1.Patients who weigh less than the 5th percentile or greater than the 95th percentile
  • 2.Patients with severe cardiovascular, neurological, hepatic, or renal impairment
  • 3.Patient with a known allergy to any of the drugs involved in the study such as propofol (and its composition; soybean oil, egg, etc.), midazolam, fentanyl, cis-atracurium, lidocaine and ondansetron
  • 4.Children with lower or upper respiratory tract infection having purulent nasal discharge, fever, or a cough
  • 5.Patients with abnormal lipid or carbohydrate metabolism
  • 6.Patients who being on anticonvulsants or psychiatric medications
  • 7.Patients who require supplemental regional anesthesia or peripheral nerve block for pain control

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