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临床试验/RPCEC00000005
RPCEC00000005已完成2 期

Evaluation of the neuroprotector effect of an extract of stem bark of Mangifera indica L. (Vimang®) in patient with Spinocerebellar Hereditary Ataxia Type 2

Center of Pharmaceutical Chemistry0 个研究点目标入组 20 人开始时间: 2009年3月13日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled trial. Masking: Double Blind. Control group: Placebo. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
18 years 至 60 years(—)
性别
All

入选标准

  • 1.Patients with diagnosis of SCA2 of any sex from 18 up to 60 years old, both inclusive.
  • 2. Patient able to develop basic activities of the daily life with independence (according to Barthel scale).
  • 3. Time of evolution of the illness until or smaller than 15 years.
  • 4. Patient that voluntarily accept to participate in the clinical trial, by means of the signature of the informed consent.

排除标准

  • 1.Patients with antecedents of alcoholism.
  • 2. Patients with antecedents of any other illness with repercussion in the nervous system.
  • 3. Patient with non controlled chronic illnesses.
  • 4. Pregnancy or nursing.
  • 5. Patient with renal or hepatic failure.
  • 6. Patients with inmunosupresores tratment or with other antioxidant treatment.
  • 7. Patients that participate in another clinical trial.

研究者

发起方
Center of Pharmaceutical Chemistry

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