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临床试验/NCT03005249
NCT03005249Unknown不适用

Neural Stem Cells Therapy for Cerebral Palsy: a Prospective, Randomized, Parallel-controlled Trial

The First Affiliated Hospital of Dalian Medical University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
20
试验地点
1
主要终点
GMFM-88 score

研究概览

简要总结

To evaluate the safety and efficacy of neural stem cells (NSCs) therapy for cerebral palsy.

详细描述

Cerebral palsy is the most severe lifelong disability disease in childhood. In China, an epidemiological investigation of cerebral palsy in 2004 has reported that 2.74‰ (about 6.50-9.75 million) of children suffered from cerebral palsy. The costs of medical expenses, living allowance and nursing care can go up to RMB 20000-50000 yuan per year for each child with cerebral palsy and thus China will expend RMB 120-300 billion yuan per year for children with cerebral palsy. With full liberalization of two-child policy, there is an increasing number of second babies born to women who are 35 years or older. Thus, the incidence of cerebral palsy tends to increase. There is currently no cure for cerebral palsy, resulting in a heavy burden for families and on society. Recent clinical trials performed in countries outside China have demonstrated that stem cell therapy is likely the most effective method to treat cerebral palsy. Fifteen trials regarding stem cell therapy for cerebral palsy have been registered with ClinicalTrials.gov. In China, there have been no standardized registered trials regarding stem cell therapy for cerebral palsy, which greatly restricts its clinical application. In October 2016, the National Health and Family Planning Commission and the Food and Drug Administration of China jointly announced the premier stem cell clinical research institutions, making performing standardized trials regarding stem cell therapy for cerebral palsy in China possible.

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
Double (Participant, Investigator)

入排标准

年龄范围
1 Year 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Neonates with ischemic/hypoxic cerebral palsy (mainly including neonate with asphyxia and premature infants);
  • Clinical manifestation of spastic tetraplegia;
  • With moderate to severe cerebral palsy, The Gross Motor Function; Classification System (GMFCS) levels IV-V;
  • Age 1-5 years, of either sex;
  • Provision of signed informed consent by one of his/her parents or legal guardians prior to commencement of this study;

排除标准

  • Systemic diseases that possibly influence treatment or patient's compliance;
  • Potentially life-threatening diseases involving various organ systems;
  • Brain deformity;
  • Abnormal behaviors or mood disorder;
  • Allergies from blood products;
  • Suffering from infectious disease;
  • Subjected to craniocerebral operations prior to screening.

研究组 & 干预措施

neural stem cells therapy group

Experimental

The patients will be assigned to neural stem cells therapy group for cerebral palsy.

干预措施: neural stem cells therapy group (Procedure)

the control group

Experimental

The patients will be assigned to the control group for cerebral palsy.

干预措施: the control group (Other)

结局指标

主要结局

GMFM-88 score

时间窗: changes of month 1, month 3, month 6, month 9 and month 12 after therapy

To evaluate change in gross motor function in children with cerebral palsy.

次要结局

  • Fine Motor Function Measure (FMFM) score(changes of month 1, month 3, month 6, month 9 and month 12 after therapy)
  • Modified Ashworth Scale score(changes of month 1, month 3, month 6, month 9 and month 12 after therapy)

研究者

发起方
The First Affiliated Hospital of Dalian Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Liu Jing

Chief Physician

The First Affiliated Hospital of Dalian Medical University

研究点 (1)

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