Effects of Repeated Use of Botulinum Neurotoxin Type A (BoNT/A) Free of Complexing Proteins in the Spastic Equinovarus Foot in Stroke Patients: A Randomized Clinical Trial
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Change in walking speed
研究概览
简要总结
Clinical randomized clinical trial to assess the effectiveness on walking speed of repeated use of botulinum neurotoxin type A (BoNT/A)in the post-stroke spastic equinovarus foot in three successive infiltrations at 6-month intervals, checking if the sustainability of the effect is greater in incobotulinumtoxin A (Xeomin®) than in onabotulinumtoxinA (Botox®).
详细描述
Spasticity is present in 38% of patients at six months after stroke. Equinovarus foot, with or without claw toes and striatal foot, is especially common. There is a weak to moderate evidence in favor of the use of botulinum neurotoxin type A (BoNT/A) in the equinovarus foot, stiff-knee and in other patterns that may interfere with gait ability. Specifically, BoNT/A increases walking speed in stroke patients with spastic equinovarus foot.
Repeated use of BoNT/A may lead to the appearance of neutralizing antibodies, so its effect may decrease over successive infiltrations. Among the differential characteristics of incobotulinumtoxinA (Xeomin®) there is a reduced inactivated botulinum neurotoxin content and the lack of complexing proteins, which would diminish antigenicity and not suppose a decrease of the effect before successive infiltrations.
The objective of this project is to determine the effect on walking speed of repeated use of BoNT/A in post-stroke spinal equinovarus foot in three consecutive injections at 6-month intervals and to investigate whether the sustainability of the effect is greater in incobotulinumtoxinA (Xeomin®) than in onabotulinumtoxinA (Botox®). All patients will receive 200-300 units of BoNT/A (Xeomin ® or Botox ®) that will be distributed according to the individual clinical pattern of spastic equinovarus foot.
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
- Double (Participant, Outcomes Assessor)
盲法说明
Double blind
入排标准
- 年龄范围
- 18 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •First-ever Ischemic or haemorrhagic stroke
- •Time since stroke onset: >6months
- •Hemiparesis with equinovarus foot
- •No previous BoNT/A
排除标准
- •Non-ambulant patients
- •Medical contraindications for BoNT/A use that appear in the product information sheet
研究组 & 干预措施
IncobotulinumtoxinA
Injection of 200-300 units of IncobotulinumtoxinA (Xeomin ®)
干预措施: IncobotulinumtoxinA (Drug)
OnabotulinumtoxinA
Injection of 200-300 units of onabotulinumtoxiA (Botox®)
干预措施: OnabotulinumtoxinA (Drug)
结局指标
主要结局
Change in walking speed
时间窗: Baseline and monthly during 18 months
Walking speed, expressed in m/s, is assessed in a 10-m corridor
次要结局
- Change in step length(Baseline and monthly during 18 months)
- Change in spasticity assessed with the Modified Ashworth Scale(Baseline and monthly during 18 months)
- Change in walking disability assessed with the Scandinavian Stroke Scale(Baseline and monthly during 18 months)
- Change in functional ambulation ability assessed with the Modified Walking Categories(Baseline and monthly during 18 months)
- Change in step time(Baseline and monthly during 18 months)
研究者
Esther Duarte
Rehabilitation Research Group Coordinator, PhD
Parc de Salut Mar
