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临床试验/EUCTR2013-002428-17-DK
EUCTR2013-002428-17-DK进行中(未招募)不适用

urse Administered Propofol Sedation vs combined sedation with midazolam/fentanil for colonoscopy in patients with IBD. A randomised controlled trial of satisfaction and adhearence to treatment program. - Propofol vs. standard sedation for colonoscopy. A study on satisfaction

Gastroenheden D, Herlev Hospital0 个研究点开始时间: 2013年10月22日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Elective endoscopy due to IBD or suspected IBD
  • 2. Willing to be randomised
  • 3. Provide written informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 170
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 30

排除标准

  • 1. Allergy to contents administered
  • 2. pregnant or nursing
  • 3. <18 years of age
  • 4. Not able to complete questionnaire
  • 5. Acute condition
  • 6. severe COPD
  • 7. > ASA II
  • 8. Sleep apnea
  • 9. Risk of aspiration
  • 10. Previously difficulty with anesthesia
  • 11. Difficult airway

研究者

发起方
Gastroenheden D, Herlev Hospital

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