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临床试验/NCT02025972
NCT02025972已完成不适用

Changes in Cytokines and Functional Outcomes of Allogeneic Cord Blood Therapy in Children With Cerebral Palsy

MinYoung Kim, M.D.2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2013年12月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
10
试验地点
2
主要终点
Changes in Standardized Gross Motor Function

研究概览

简要总结

This open-label study aims to analyze cytokines related to clinical outcomes of allogeneic umbilical cord blood therapy for children with cerebral palsy.

详细描述

Cerebral palsy (CP) is a group of neurodevelopmental conditions with abnormal movement and posture resulted from a non-progressive cerebral disturbance. It is the most common cause of motor disability in childhood. Most therapies are palliative rather than restorative. Umbilical cord blood (UCB) may be used as restorative approach for children with CP.

Many experimental animal studies have revealed that UCB is beneficial to improve and repair neurological injuries.

Based on animal studies and some clinical trials, UCB is suggested as a potential therapy for children with CP. This study was designed to find cytokines relevant to UCB therapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with cerebral palsy
  • Age of ≤15 years
  • Mismatch in HLA-A, B, and DR ≤2, and total nucleated cell count ≥3x10^7/kg. If the cell count is less than given values, more than 1 unit could be used.
  • Decision of participation in the study by and acquisition of informed consent from the subject's representative
  • Willingness and ability to be hospitalized according to the schedule specified in the protocol and continue the study for 12 months after study entry

排除标准

  • Current aspiration pneumonia
  • Known genetic disease
  • History of hypersensitivity reaction to any study drugs pertinent to the study
  • Patient with severe seizure disease who has clinical convulsion despite combination therapy with 3 or more agents
  • Uncontrolled hypertension defined as systolic blood pressure >115 mmHg and/or diastolic blood pressure >70 mmHg
  • Hepatic impairment defined as asparate aminotransferase (AST) >55 IU/L and/or alanine aminotransferase (ALT) >45 IU/L
  • Renal impairment defined as creatinine (Cr) ≥1.2 mg/dL
  • Presence of diagnosed or suspected malignant tumor and/or hematologic malignancy
  • Non-compliance with study visits specified in the protocol or unwillingness of care-giver due to lack of understanding of the patient

研究组 & 干预措施

Allogeneic umbilical cord blood therapy

Experimental

Allogeneic umbilical cord blood therapy

干预措施: Allogeneic umbilical cord blood therapy (Procedure)

结局指标

主要结局

Changes in Standardized Gross Motor Function

时间窗: Baseline - 3 months - 6 months - 12months

GMFM (Gross Motor Function Measure) is a standardized measurement tool for assessing gross motor function consisting of sub-scales; lying \& rolling, sitting, crawling \& kneeling, standing, walking, running \& jumping (range: 0\~100, higher value means better gross motor function).

Changes in Motor Neurodevelopmental Outcome

时间窗: Baseline - 3 months - 6 months - 12 months

Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Motor Scale (range: 0\~112; worst: 0, best: 112)

Cytokine analysis

时间窗: 12 months

Cytokine analysis

Changes in Cognitive Neurodevelopmental Outcome

时间窗: Baseline - 3 months - 6 months - 12 months

Korean version of Bayley Scale of Infant Development-II (K-BSID-II) Mental Scale (range: 0\~178; worst: 0, best: 178)

Changes in Motor Performance

时间窗: Baseline - 3 months - 6 months - 12 months

GMPM (Gross Motor Performance Measure) is a standardized measurement tool for assessing quality of movement regarding 3 properties of 5 ones; alignment, coordination, dissociated movement, stability, and weight shift (range: 0\~100, higher value means better motor quality).

次要结局

  • Changes in Gross Motor Function Classification System(Baseline - 3 months - 6 months - 12 months)
  • Changes in Functional Independence in Daily Activities(Baseline - 3 months - 6 months - 12 months)
  • Changes in Visual Perception Test(Baseline - 3 months - 6 months - 12 months)
  • Changes in Dynamic Component of Spasticity(Baseline - 3 months - 6 months - 12 months)
  • Changes in Brain 18F-FDG PET(Baseline - 12 months)
  • Changes in Upper Extremity Function(Baseline - 3 months - 6 months - 12 months)
  • Changes in Selective Movement of Lower Extremity(Baseline - 3 months - 6 months - 12 months)
  • Changes in Spasticity(Baseline - 3 months - 6 months - 12 months)
  • Changes in EP(Baseline - 12 months)
  • Changes in Brain MRI(Baseline - 12 months)
  • Number of adverse events and participants with those adverse events(12 months)
  • Changes in Functional Performance in Daily Activities(Baseline - 3 months - 6 months - 12 months)
  • Changes in Muscle Strength(Baseline - 3 months - 6 months - 12 months)
  • Changes in EEG(Baseline - 12 months)

研究者

发起方
MinYoung Kim, M.D.
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

MinYoung Kim, M.D.

Professor of CHA University, M.D., Ph.D.

Bundang CHA Hospital

研究点 (2)

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