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临床试验/ISRCTN38393880
ISRCTN38393880已完成2 期

Add-on treatment with Cerebrolysin improves clinical symptoms in amyotrophic lateral sclerosis patients: results of a prospective, single-center, placebo-controlled, randomized, double-blind, Phase II study

Instituto Cardiológico Banfield0 个研究点目标入组 20 人开始时间: 2024年1月8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

入排标准

性别
All

入选标准

  • 1. Either sex and at least 18 years of age
  • 2. Clinically definite diagnosis of ALS according to the El Escorial and revised Airlie House diagnostic criteria
  • 3. Limb onset and/or bulbar onset with pyramidal signs
  • 4. Modified Ashworth Spasticity Scale score of 3
  • 5. Informed consent

排除标准

  • 1. Co-morbidities such as hepatic disease, renal failure or severe renal impairment, coronary disease, epilepsy, Parkinson’s disease, or dementia
  • 2. Any condition that might interfere with compliance with study procedures or influence outcome assessment
  • 3. Pregnant or breastfeeding
  • 4. Participation in another interventional study within the previous 2 months
  • 5. Contraindication to Cerebrolysin
  • 6. Concomitant use of ginkgo biloba, erythropoietin, citicoline, and amantadine

研究者

发起方
Instituto Cardiológico Banfield

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