跳至主要内容
临床试验/EUCTR2006-000875-14-BE
EUCTR2006-000875-14-BE进行中(未招募)不适用

Short-, and long-term effects of the intra-operative nitrous oxide administration on the remifentanil-induced post-operative hyperalgesia, morphine consumption and long-term quality of life - nitrous oxide administration on the post-operative hyperalgesia

AIR LIQUIDE SANTE INTERNATIONA0 个研究点目标入组 138 人开始时间: 2006年7月7日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
138

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

  • - types of surgery interventions: major abdominal surgeries with laparotomy of expected length of 4 hours or even specified
  • - adults: 18 to 65 years old
  • - ASA 1-3
  • - signed patient consent form
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Thoracic surgery
  • -Psychotropic agent chronic usage
  • -Chronic pain or chronic use of opioid analgesic
  • -Preceding major abdominal surgery
  • -Expected prolonged intubation
  • -Radiation in the area of surgery
  • -Regular intake of analgesics (except low dose acetylic acid for cardiovascular reasons)
  • -Opioid intake 24 hours before surgery
  • -Major obesity (BMI > 30)
  • -Drug or alcohol abuse
  • -Incapability of handling of PCA
  • -Instable or significant central nervous system, cardiac, hepatic, renal or endocrine dysfunction and/or significant sequelas
  • -Product-related exclusion criteria.

研究者

发起方
AIR LIQUIDE SANTE INTERNATIONA

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