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临床试验/NL-OMON45146
NL-OMON45146已完成不适用

Sedation with propofol TCI during ERCP: Is the combination with esketamine more effective and safer than with alfentanil (SPEKA): A randomized controlled multicentre trial - SPEKA

Academisch Medisch Centrum0 个研究点目标入组 166 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
166

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 至 99(—)

入选标准

  • The patients must comply with the following criteria in order to be eligible to participate in this clinical study:;Age range * 18 years
  • ASA classification I * III
  • Planned ERCP/EUS procedure
  • Written informed consent

排除标准

  • Patient will be excluded if the following criteria are applicable:
  • Age range< 18 years
  • ASA classification IV and V
  • Allergic reaction to planned medication in the patients* medical history
  • Unregulated hypertension
  • History of malignant hypertension
  • Significant ischaemic heart disease
  • Mentally disordered
  • History of psychological problems or psychiatric disease
  • Use of drugs that affect the central nervous system
  • Substance abuse
  • Chronic pain
  • Seizure disorders
  • Increased intracranial pressure

研究者

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