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临床试验/IRCT20200818048445N1
IRCT20200818048445N1招募中2 期

A Comparison between the effect of Propofol Fentanyl and Propofol Ketamine on Colonoscopy patients' sedation.

Ahvaz University of Medical Sciences0 个研究点目标入组 144 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
144

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

  • They are between 18 and 65 years old
  • Patients are referred for colonoscopy procedure
  • Classification of Group 1 and 2 American Society of Anesthesiologists (ASA Class I & II) are selected as inclusion criteria.

排除标准

  • the patient's unwillingness to participate in the study
  • They are under 18 years old
  • They are over 65 years old
  • They have kidney failure
  • They have liver failure
  • They have chronic pain syndrome
  • They are addicted
  • They have any drug allergies
  • They have cardiovascular disease
  • They have a respiratory disease
  • They have metabolic diseases
  • They have a neurological disease
  • They have difficult airways
  • The patient is classified as ASA class 3 and 4
  • Contraindicated propofol ketamine or propofol fentanyl

研究者

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