跳至主要内容
临床试验/NCT01016119
NCT01016119已完成3 期

Efficacy of Folrex in the Superior Extremity Rehabilitation After Acute Stroke

Catalysis SL1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2009年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Catalysis SL
入组人数
40
试验地点
1
主要终点
Periodical measures of the motor recovery, of the upper extremity, by Fugl-Meyer score, it will be done at the beginning, at fifth day and at month (4 weeks).

研究概览

简要总结

The purpose of the study is to evaluate whether Folrex, could improve the motor recovery of the upper extremity after stroke in comparison with placebo during 4 weeks of treatment.

详细描述

Periodical measures of the motor recovery, of the upper extremity, by Fugl-Meyer score, it will be done at the beginning, at fifth day and at month. Each value will be compare to evaluate whether the groups of patient improve.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with acute stroke < 24 hours.
  • Patients with impairment up to 4 on NIHSS scale.
  • Family support.
  • Informed consent.

排除标准

  • Presence of another disease not well controlled.
  • Patient with dementia.

研究组 & 干预措施

Placebo

Placebo Comparator

In this group we will use Placebo cream, in the early rehabilitations in the upper extremity

干预措施: Placebo (Drug)

Folrex

Experimental

In this group we will use Folrex cream, in the early rehabilitations in the upper extremity

干预措施: Folrex (Drug)

结局指标

主要结局

Periodical measures of the motor recovery, of the upper extremity, by Fugl-Meyer score, it will be done at the beginning, at fifth day and at month (4 weeks).

时间窗: 4 weeks

次要结局

  • Barthel index(4 weeks)
  • National Institutes of Health Stroke Scale (NIHSS)(4 weeks)

研究者

发起方
Catalysis SL
申办方类型
Industry

研究点 (1)

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