TCTR20220829001已完成2 期
The randomized, double-blinded, controlled trial of Kaempferia parviflora versus Betahistine in treating chronic vertigenous patients
Argricultural Research Development Agency (Public Organization)0 个研究点目标入组 38 人开始时间: 2022年8月29日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 38
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 75 Years(—)
- 性别
- All
入选标准
- •1. Individual who suffered from chronic dizziness longer than 1 month with DHI-T score over 18
- •2. Age 18-75 years
- •3. Individual who are willing and able to comply with protocol until the end of project
- •4. Able to read and write in Thai
排除标准
- •1. Individual who had been diagnosed with Benign Paroxysmal Positional Vertigo or Vestibular Migraine or Height Vertigo or Orthostatic Hypotension or Mental or psychiatric problem
- •2. Individual with abnormal proprioception including tremor and hemiplegia paraplegia
- •3. Individual with cardiac arrythmia
- •4. Individual who had been treated with and cannot withdraw EGb761 120mg/day or over or Betahistine 36 mg/day or over for longer than 72 hours
- •5. Individual who currently consume other herbal medicines
- •6. Individual who currently consume any kind of neurotic suppressor medications
- •7. Individual with active otitis media or perforation of tympanic membrane
- •8. Individual with abnormal liver and kidney function (GFR lower than 60)
- •9. Individual who cannot sit or stand without assistant
- •10. Individual with urine pregnancy test positive or in pregnancy condition
研究者
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