跳至主要内容
临床试验/NCT03624283
NCT03624283Unknown不适用

The Effect of Vestibular Exercise, With or Without Medication, in Managing Residual Dizziness After Successful Repositioning Maneuvers in Patients With Benign Paroxysmal Positional Vertigo

Eye & ENT Hospital of Fudan University1 个研究点 分布在 1 个国家目标入组 183 人开始时间: 2018年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
183
试验地点
1
主要终点
Balance function

研究概览

简要总结

To investigate the effect of vestibular rehabilitation, with or without medication, on resolving residual dizziness after successful repositioning maneuvers in patients with benign paroxysmal positional.

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, Outcomes Assessor)

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

入选标准

  • Diagnosed as unilateral BPPV (unilateral posterior semicircular canal BPPV or horizontal semicircular canal BPPV) according to the clinical practice guideline issued by American Academy of Otolaryngology and head and neck surgery (AAO-HNSF) in 2017;
  • Aged 18~80 years;
  • Reporting residual symptoms after successful repositioning maneuvers;

排除标准

  • Anterior semicircular canal BPPV or multicanal BPPV;
  • Recurrent BPPV;
  • Subjects with coexisting vestibular disorders, including Meniere disease, vestibular neuritis, labyrinthitis, and peripheral vestibular loss;
  • Subjects with severe cervical spine disease;
  • Subjects with severe cardiovascular diseases ;
  • Subjects with known cerebral vascular disease like carotid stenosis;
  • Cognitive impairment;
  • Suspect of significant depression or anxiety as defined as a score of ≥ 8 for each respective scale of Hospital anxiety and depression scale;
  • Pregnant/ lactating or planning to become pregnant during the study period;
  • Had taken vestibulosupressant, antihistamines, and/ or ototoxic medications in the past 3 months;

研究组 & 干预措施

Group C

Experimental

Group C will receive an combination of Exercise-based VR plus Betahistine.

干预措施: Exercise-based vestibular rehabilitation (Behavioral)

Group A

Experimental

Group A will be provided with Exercise-based vestibular rehabilitation (VR) twice per day for a period of 4 weeks;

干预措施: Exercise-based vestibular rehabilitation (Behavioral)

Group B

Experimental

Group B will be prescribed with Betahistine 12mg, twice daily for 7 days;

干预措施: Betahistine (Drug)

Group C

Experimental

Group C will receive an combination of Exercise-based VR plus Betahistine.

干预措施: Betahistine (Drug)

结局指标

主要结局

Balance function

时间窗: Change from baseline, at 4 weeks, 8 weeks and 12 weeks postrandomisation

Balance function, measured by computerized dynamic posturography.

次要结局

  • Duration of RD symptoms(Change from baseline at 4 weeks, 8 weeks and 12 weeks postrandomisation.)
  • Quality of life assessment scale(Change from baseline at 4 weeks, 8 weeks and 12 weeks postrandomisation.)
  • Otolith function(Change from baseline at 4 weeks, 8 weeks and 12 weeks follow-up will be necessary only when the previous examine showing abnormal.)
  • Daily function(Change from baseline, at 4 weeks, 8 weeks and 12 weeks postrandomisation)

研究者

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

Huawei Li, Ph.D, MD

Director of Otorhinolaryngology

Eye & ENT Hospital of Fudan University

研究点 (1)

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