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临床试验/NCT02475239
NCT02475239Unknown不适用

Efficacy of Postural Restriction in Treating Benign Paroxysmal Positional Vertigo

Prince of Songkla University1 个研究点 分布在 1 个国家目标入组 186 人开始时间: 2014年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
186
试验地点
1
主要终点
The Dix-Hallpike test

研究概览

简要总结

The standard treatment of posterior semicircular canal benign paroxysmal positional vertigo is the canalith repositioning procedure or the Epley maneuver. Based on the present literature, there is controversy on the efficacy of post-maneuver postural restrictions.The aim of this study was to conduct a randomized controlled trial to compare the treatment efficacy of post-maneuver postural restriction with CRP alone in patients with posterior semicircular canal benign paroxysmal positional vertigo.

详细描述

Benign paroxysmal positional vertigo is the most common cause of vertigo. Based on the present literature, there is controversy on the efficacy of post-maneuver postural restrictions.Some study designs were not randomized controlled trials. The present study offers an alternative way of postural restriction to maintain postural restriction as much as possible.

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
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with unilateral posterior semicircular canal benign paroxysmal positional vertigo and
  • •A negative neurologic examination

排除标准

  • •Secondary benign paroxysmal positional vertigo caused by trauma head injury, inner ear surgery, viral labyrinthitis or Meniere's disease
  • •Patients with central vertigo, cervical spine, neurologic, otologic, psychiatric diseases
  • •Patients who used medications that affected the neurologic and otologic systems for less than 48 hours

研究组 & 干预措施

Postural restriction

Experimental

The patients were instructed to avoid head movements, wear a soft collar during the daytime, wear a supporting pillow and sleep in the semi-upright position at a 45 degree head elevation from the horizontal plane during the nighttime for 48 hours.

干预措施: Postural restriction (Behavioral)

Normal daily activity

Active Comparator

The patients did not follow any postural restrictions and were asked to live as normally as possible.

干预措施: Normal daily activity (Behavioral)

结局指标

主要结局

The Dix-Hallpike test

时间窗: 2 weeks

The Dix-Hallpike test results

次要结局

  • Recurrent rate(24 weeks)
  • Resolution time(24 weeks)
  • Medication needed(24 weeks)
  • the Dizziness Handicap Inventory (DHI)(24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yuvatiya Plodpai

Doctor

Prince of Songkla University

研究点 (1)

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