跳至主要内容
临床试验/NCT02709876
NCT02709876Unknown1 期

Autologous Bone Marrow-Derived CD34+, CD133+, and CD271+ Stem Cell Transplantation for Retinitis Pigmentosa

Stem Cells Arabia2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2014年4月最近更新:
适应症

试验速览

阶段
1 期
入组人数
50
试验地点
2
主要终点
ETDRS Visual acuity change

研究概览

简要总结

A single arm, single center trial to evaluate the safety and efficacy of autologous purified populations of bone-marrow derived stem cells in patients with Retinitis Pigmentosa (BM-SCs) through a 48 month follow up period.

详细描述

Retinitis pigmentosa (RP) is an inherited disorder of the photoreceptor cells in the retina. Patients may lose vision since they were young or later in life. Currently, there are more than 60 genes identified as the cause of this condition, one of which, RPE65, has been studied in several gene therapy trials for Leber congenital amaurosis with promising results. Another treatment approach for RP is stem cell therapy. Studies in animal models of RP have shown that subretinal injection of bone marrow-derived mesenchymal stem cells may delay degenerative changes of photoreceptor cells. This is a single arm, single center trial to assess the safety and efficacy of purified adult autologous bone marrow derived CD34+, CD133+, and CD271+ stem cells through a 48 month follow-up period. The combination of these three cell types was based on their diverse potentialities to differentiate into specific functional cell types to regenerate damaged retinal tissue, and the availability of clinical-grade purification system (CliniMACS) and microbeads to purify the target cell populations in clinically-approved methods.

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
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Retinitis pigmentosa patients diagnosed by ophthalmologists
  • Visual acuity (measured with ETDRS) less than or equal to 20/70 and visual field below 30° central in both eyes.
  • Best corrected visual acuity less than 6/120 by Snellen visual acuity chart

排除标准

  • Other eye conditions that could mask the interpretation of the results
  • Unable to return for follow up
  • Underlying diseases including asthma, heart failure, myocardial infarction, liver failure, renal failure
  • Pregnant and lactating women

结局指标

主要结局

ETDRS Visual acuity change

时间窗: 12 months from baseline

次要结局

  • Color Vision: Ishihara Color Test(12 months from baseline)
  • Quality of Life: Questionnaire VFQ-25 (Visual Function Questionnaire-25)(12 months from baseline)
  • Contrast sensitivity: CSV-1000E(12 months from baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验