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
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