跳至主要内容
临床试验/EUCTR2018-002295-40-DK
EUCTR2018-002295-40-DK进行中(未招募)1 期

Pharmacokinetics and safety of treatment with paracetamol in children and adults with spinal muscular atrophy and cerebral palsy - Paracetamol study in patients with low muscle mass

Copenhagen Neuromuscular Center0 个研究点目标入组 24 人开始时间: 2018年7月11日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
24

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

  • -Patients: Men, women and children diagnosed with/biochemically verified SMA and CP
  • -Patients admitted to the ICU: Men, women, children diagnosed with/biochemically verified SMA and CP
  • -Healthy controls: Need to be healthy, evaluated by the investigator.
  • oChildren: 6-18 years
  • oAdult patients: 18-45 years
  • oHealthy controls: 18-45 years
  • oICU-admitted patients: 6-45 years
  • -Signed informed consent to participation in the trial
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 12
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 12
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Inability to understand the purpose of the trial or cooperate in the conduction of the experiments.
  • oFor the children this will concern of course the parents or the guardians of the child.
  • -Competing conditions at risk for compromising the results of the study.
  • -Participation in other trials that may interfere with the results.
  • -Intake of medications that may interfere with the results, evaluated by investigator.
  • -Pregnancy and breastfeeding.

研究者

发起方
Copenhagen Neuromuscular Center

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