跳至主要内容
临床试验/EUCTR2005-003887-48-GB
EUCTR2005-003887-48-GB进行中(未招募)1 期

Randomised Controlled Trial of patient-controlled sedation for colonoscopy: Entonox versus target-controlled infusion of propofol - RCT of patient controlled sedation for colonscopy

HULL AND EAST YORKSHIRE NHS TRUST0 个研究点目标入组 0 人开始时间: 2005年10月25日最近更新:
适应症
相关药物

试验速览

阶段
1 期
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

入选标准

  • All patients of both sexes undergoing elective colonoscopy will be recruited
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Patients with chronic pulmonary disease,
  • 2. History of colonic resection,
  • 3. Intolerance to any of the drugs,
  • 4. Unwilling to enter the trial
  • 5. ASA class IV,
  • 6. Allergy to soybeans, eggs,
  • 7. History of seizure disorder, sleep apnoea, or difficult intubation, a short thick neck, and inability to open mouth widely.

研究者

发起方
HULL AND EAST YORKSHIRE NHS TRUST

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