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临床试验/KCT0008667
KCT0008667招募中Unknown

Comparison of efficacy and safety of remimazolam and propofol: multicenter prospective randomized trial

Yonsei University Health System, Gangnam Severance Hospital0 个研究点目标入组 394 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
发起方
入组人数
394

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
20(Year) 至 o Limit(—)
性别
All

入选标准

  • 1) Men or women between the ages of 20 and 70
  • 2) Subjects who have voluntarily decided to participate after hearing the explanation of the clinical trial process and signed the consent form
  • 3) All subjects requiring ultrasound endoscopy
  • 4) Subjects with class I or II in the American Society of Anesthesiology (ASA) risk assessment

排除标准

  • 1) Pregnant woman
  • 2) Those who are susceptible to remimazolam, propofol or benzodiazepine drugs (midazolam), or those who are susceptible to eggs, beans, etc
  • 3) subjects undergoing adrenocortical or chronic steroid therapy or porphyria
  • 4) Subjects who are expected to have difficulty with airway intubation (subjects who have difficulty opening their mouths wide or have a thick neck and short neck)
  • 5) a subject diagnosed with sleep apnea
  • 6) Subjects with a history of reported risk cases during sedative endoscopy in the past
  • 7) Subjects with severe renal disease (serum creatinine >2 mg/dL)
  • 8) Subjects with severe heart disease (subjects with NYHA class III or IV)
  • 9) subjects who wish to receive an endoscopy without sincerity
  • 10) Subjects who cannot or are not willing to prepare an automatic test protocol or who do not agree to provide information;
  • 11) Subjects whose oxygen saturation is less than 90% or less than 95% despite the oxygen supply of 2 L/min
  • 12) Subjects with an underlying systolic blood pressure of less than 80 mmHg

研究者

发起方
Yonsei University Health System, Gangnam Severance Hospital

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