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临床试验/IRCT20150206020981N4
IRCT20150206020981N4招募中2 期

Evaluation of safety and efficacy of focal intramuscular injection of wharton’s gelly-derived mesenchymal stem cell in Duchenne muscular dystrophy pediatrics between 5 to 12 years old

Sinacell Company0 个研究点目标入组 5 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
5

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
5 years 至 12 years(—)
性别
Male

入选标准

  • Age between 5 to 12
  • Genetic evidence of Duchenne disease as a cause of myopathy
  • The patient's ability to walk is not completely lost and the use of assistive devices such as canes and walkers is not permanent.
  • The patient's muscle strength is decreasing
  • Willingness and satisfaction to participate in the study by the patient's legal guardian in decision making and willingness to participate regularly in follow-up courses
  • Weight between 15 to 35

排除标准

  • Advanced motor impairment leading to permanent use of crutches, walkers and wheelchairs
  • A history of known malignancy
  • History of associated genetic and non-genetic degenerative diseases
  • A history of any other acute or chronic illness that, at the discretion of the clinician responsible for implementing the plan, prevents the patient from entering the study.

研究者

发起方
Sinacell Company

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