CTIS2024-510866-18-00进行中（未招募）1 期
Comparative study of the mechanism of action of Dry Needling and Botulinum Toxin type A as a treatment for lower limb post-stroke spasticity: a proof of concept controlled trial - 49317
未提供0 个研究点目标入组 60 人开始时间: 2024年3月29日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 年龄范围
- 18 至 65+（—）
- 性别
- All
入选标准
- •aged 18-85 years old, having lower limb post-stroke spasticity in ankle plantar flexors (MAS scores of 1, 1+ and 2);, having had a first stroke, having no more than 12 months of evolution since stroke; 5) having no previous Dry Needling (DN) or Botulinum Toxin type A (BTX A) treatment for spasticity, having ankle PROM = 20° (approx.) when the knee is supported in ~30° flexion, being able to walk independently with or without aids, having no previous Dry Needling (DN) or Botulinum Toxin type A (BTX A) treatment for spasticity
排除标准
- •medical conditions interfering with data interpretation, any contraindication to receiving BTX A or PS treatment, If taking anti-spasticity medications, participants must be on stable medication for at least 3 months prior to the start of the study and neither the dose nor the medication can be changed during the trial, Pregnancy and/or Breastfeeding
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