NCT00978809撤回不适用
Epley Maneuver vs. Semont Maneuver for Benign Paroxysmal Positional Vertigo (BPPV): Evaluating Treatment Effectiveness by Postural Stability - a Double Blinded Randomized Controlled Trial.
Assuta Hospital Systems1 个研究点 分布在 1 个国家开始时间: 2009年9月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 试验地点
- 1
- 主要终点
- postural stability
研究概览
简要总结
The propose of this study is to compare two methods of physical treatment for benign paroxysmal positional vertigo, by evaluating treatment effects on postural stability.
The trail design is a double blinded randomized controlled trail, with each patient going through three evaluations: before treatment, 1 week after treatment and 60 days after treatment.
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 (Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •medical referral for treating "vertigo"
- •subject has short episodes of rotatory vertigo (up to 1 minute)
- •subject has positive Hallpike-Dix test with typical nystagmus
- •repeated Hallpike-dix test will show fatigability
排除标准
- •Hallpike-Dix test produces vertigo without nystagmus
- •subject has BPPV of the horizontal or anterior semi-circular canal
- •subject has other known vestibular or neurologic condition
- •subject has nystagmus of a different type
- •subject has a cervical spine problem which prevents the utilization of Epley or Semont maneuvers
- •subject is unable to stand for 1 minute
- •subject gets pharmacologic treatment for vertigo while doing the postural stability evaluation
- •subject is under 18 years old or a pregnant female or cannot obtain informed concent
结局指标
主要结局
postural stability
时间窗: 60 days post treatment
次要结局
- subjective vertigo(60 days post treatment)
研究者
研究点 (1)
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