NCT06007573已完成不适用
Acupuncture Combined With Nimodipine for Prevention of Post-stroke Dementia:a Randomized Controlled Trial
Yuzhen Pan1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年2月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Response Rate
研究概览
简要总结
To observe the clinical efficacy of TCM acupuncture combined with western medicine nimodipine for prevention of post-stroke dementia by comparing with clinical conventional treatment methods.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 40 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Definite ischemic stroke or hemorrhagic stroke confirmed by head CT / MRI examination
- •Memory or cognitive and executive dysfunction. Cognitive dysfunction will be determined after the mini mental state evaluation (MMSE) score
- •Age limited to 40-85 years, irrespective of gender
- •Stable condition, clear consciousness, no aphasia, oral medication available
- •No major comorbidity, no major depression
- •Consent and signed patient informed consent
排除标准
- •Had serious medical conditions, such as heart, liver, kidney, or endocrine disease
- •Aphasia or hearing impairment
- •Participants in other clinical trials
- •Patients currently on medication to improve cognitive function
研究组 & 干预措施
treatment group
Experimental
On the basis of the control group treatment, the treatment group also adopted the acupuncture treatment
干预措施: The control group received oral nimodipine tablets (Drug)
control group
Other
The control group received oral nimodipine tablets
干预措施: The control group received oral nimodipine tablets (Drug)
结局指标
主要结局
Response Rate
时间窗: 24 weeks
次要结局
- Hasegawa Dementia Scale(24 weeks)
- Montreal Cognitive Assessment(24 weeks)
研究者
Yuzhen Pan
DOCTOR
The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine
研究点 (1)
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