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临床试验/EUCTR2006-001284-33-ES
EUCTR2006-001284-33-ES进行中(未招募)不适用

pain relief management by kalinox 170 bar for short-time painful procedure in paediatric patientsalivio del dolor con kalinox 170 bar en pacientes pediatricos sometidos a procedimientos dolorosos de corta duracion - pain relief management in paediatric patients

air liquide sante international0 个研究点目标入组 150 人开始时间: 2006年5月25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)
入组人数
150

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

  • - paediatrics patients, aged 1 to 18 years-
  • Able to use a Revised FACES Pain Scale (patient > 6 years)
  • -Able to be applied a Spanish Observational Pain Scale LLANTO SCALE” (patient < 6 years)
  • -Short-term painful procedures in the following paediatrics groups : cutaneous, burned, bone and joints, endoscopy
  • -Signed informed consent
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • 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

  • - Patient having already been included in this protocol
  • - Significant impairment in general condition (WHO > 3)
  • - Patient unable to rate pain on Revised FACES Pain Scale (patient > 6 years)
  • - Patient unable to be applied LLANTO SCALE (patient < 6 years)
  • - Confusion-
  • Product-related non-inclusion criteria

研究者

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