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临床试验/NCT02866331
NCT02866331Unknown2 期

Phase II, Randomized, Double-blind Clinical Trial for Efficacy of G-CSF and Autologous Cord Blood Infusion in Children With Cerebral Palsy

Hanyang University Seoul Hospital1 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2016年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
88
试验地点
1
主要终点
Confirm the safety of autologous cord blood infusion and repeated injection of G-CSF in children with cerebral palsy by repeated follow-up every 3 months over 18 months with clinical and laboratory evaluations

研究概览

简要总结

This study is performed to reveal the safety and feasibility of combination therapy with autologous cord blood mononuclear cells (CB) and G-CSF as well as repeated administration of G-CSF for children with cerebral palsy. The evaluation tools are as follows: (1) Developmental tests (DDST, PEDI, GMFM, GMFCS, MACS, QUEST), (2) Neurocognitive function test (WPPSI-IV), (3) Brain MRI-DTI, (4) Peripheral blood CD34+ cell counts, (5) Neurotrophic factors/anti-inflammatory cytokines.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
2 Years 至 10 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Ages from 2 years to 10 years at the time of enrollment
  • Non-severe type of cerebral palsy
  • Willing to comply with all study procedures

排除标准

  • Previous participation within 1 year in a clinical study with stem cell therapy including cord blood, G-CSF, and erythropoietin
  • Presence of chromosomal abnormalities
  • Unwillingness to participate clinical trial
  • Presence of hypersensitivity reaction to G-CSF
  • Evidence of hepatic, renal, cardiac dysfunctions

研究组 & 干预措施

CB + G-CSF

Experimental

干预措施: G-CSF (Leucostim) (Drug)

CB + G-CSF

Experimental

干预措施: CB (autologous cord blood) (Biological)

CB + placebo

Placebo Comparator

干预措施: CB (autologous cord blood) (Biological)

CB + placebo

Placebo Comparator

干预措施: Placebo (Normal saline) (Drug)

G-CSF

Experimental

干预措施: G-CSF (Leucostim) (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Normal saline) (Drug)

结局指标

主要结局

Confirm the safety of autologous cord blood infusion and repeated injection of G-CSF in children with cerebral palsy by repeated follow-up every 3 months over 18 months with clinical and laboratory evaluations

时间窗: For 18 months from date of randomization

次要结局

  • Confirm the efficacy of autologous cord blood infusion and/or G-CSF in children with cerebral palsy using standardized Gross Motor Function Measure evaluation.(Every 6 months from date of randomization up to 18 months)

研究者

发起方
Hanyang University Seoul Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Young-Ho Lee

Professor, Department of Pediatrics

Hanyang University Seoul Hospital

研究点 (1)

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