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
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