跳至主要内容
临床试验/NCT01360164
NCT01360164Unknown1 期

Phase I/II Study of Umbilical Cord Mesenchymal Stem Cell Therapy for Patients With Hereditary Ataxia

Shenzhen Beike Bio-Technology Co., Ltd.1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2010年1月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
20
试验地点
1
主要终点
the volume of Cerebellum of Brain Magnetic Resonance Imaging (MRI) Scan

研究概览

简要总结

The Hereditary Ataxias are a group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements. Current treatments for Hereditary Ataxias are mainly pharmacological, rehabilitative, or psychological treatments,while no effective treatment available. Stem Cell therapy is a novel and promising therapeutic strategy for Hereditary Ataxias treatment. In this study, the safety and efficacy of Human Umbilical Cord Mesenchymal Stem Cells transplantation will be evaluated in patients with Hereditary Ataxias.

详细描述

This Study is designed to evaluate the the safety and efficacy of Human Umbilical Cord Mesenchymal Stem Cells transplantation in patients with Hereditary Ataxias.

研究设计

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

入排标准

年龄范围
16 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 16-65 years.
  • Harding Diagnosis of SCAs, gene type confirmed.
  • Candidates who did not receive any stem cell therapy in past 6months.
  • sign the consent form and follow the clinic trail procedure.

排除标准

  • Cardiac insufficiency; Renal insufficiency; hepatic insufficiency; Total bilirubin higher than 1.5 times of upper limit of normal value; AST /ALT higher than 2.5 times of upper limit of normal value;
  • Routine Blood Test: WBC count <3.0×109/ L; PLT count <5×109/L ; or Hemoglobin <100g/L;
  • Combined Pneumonia or other Severe systemic bacteria infection;
  • Severe drug allergic history or anaphylaxis to 2 or more food or medicine;
  • Other brain organic disease (eg. Brain cancer);
  • HIV+, Tumor Markers + ;
  • Severe psychotic patients, cognitive dysfunction, or can not understand or sign the Consent Form;
  • Other severe systemic or organic disease;
  • Uncontrolled hypertension,blood pressure≥180mmHg/110 mmHg after treatment;
  • Pregnancy;
  • Enrollment in other trials in the last 3 months;
  • Other criteria the investigator consider improper for inclusion.

结局指标

主要结局

the volume of Cerebellum of Brain Magnetic Resonance Imaging (MRI) Scan

时间窗: 1 year after treatment

scores of International Cooperative Ataxia Rating Scale (ICARS) scale and Berg Scale

时间窗: 1 year after treatment

次要结局

  • Number of Participants with Adverse Events as a Measure of Safety and Tolerability(1 year after treatment)
  • Number of Participants with Serious Adverse Events as a Measure of Safety and Tolerability(1 year after treatment)

研究者

发起方
Shenzhen Beike Bio-Technology Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验