Suppr超能文献

补肾开窍方治疗阿尔茨海默病的有效性和安全性:一项多中心、前瞻性、真实世界临床试验的研究方案

Effectiveness and Safety of Bu Shen Kai Qiao Fang in the Treatment of Alzheimer's Disease: Study Protocol for a Multicenter, Prospective, Real-World Clinical Trial.

作者信息

Xu ZeYu, Li Ou, Liang YaTing, Wu ZhiBing, Xu Jiamei, Wang Ling, Li Ling, Sun YongNing

机构信息

Department of Brain and Mental Disease, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, ShangHai, 200040, People's Republic of China.

Department of Encephalopathy, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, People's Republic of China.

出版信息

Int J Gen Med. 2023 Jun 17;16:2573-2583. doi: 10.2147/IJGM.S418700. eCollection 2023.

Abstract

BACKGROUND

Alzheimer's disease (AD) is a common degenerative disease of the nervous system with serious impact on quality of life of patients and their families. With an aging population, AD has become a major public health problem in China and worldwide. However, the physiological and pathological mechanisms of AD have not been fully elucidated, and there is a lack of effective prevention and clinical treatment methods. Many studies have found that traditional Chinese medicine (TCM) has a good therapeutic effect on cognitive function in AD patients. Bu Shen Kai Qiao Fang (BSKQF) is one such Chinese herbal preparation used in the treatment of AD. We designed a protocol for a real-world clinical study of BSKQF combined with Donepezil hydrochloride (DH) to evaluate the efficacy and safety of this approach in the treatment of AD patients.

METHODS

This is a protocol for a real-world, multicenter, prospective, observational cohort study. The study will recruit 860 AD patients from four hospitals across China. Equal numbers of patients will be treated with BSKQF and DH or with DH only. The criteria for grouping are based primarily on patient preference. Outcome measures include scores on the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment Scale (MOCA) and will be recorded at baseline, and at one, two and three months after enrollment. The plasma Aβ42 and plasma Tau levels of participating patients will also be measured by ELISA at baseline and after 3 months of treatment. Safety metrics and adverse events (AEs) of participating patients will be monitored and recorded.

DISCUSSION

This study will evaluate the clinical efficacy and safety of BSKQF in the treatment of AD. The results will provide reliable evidence for the clinical application of BSKQF in the treatment of AD.

STUDY REGISTRATION

Trial registration: Chinese Clinical Trial Registry, NO. ChiCTR2000039670, Registered 5 November 2020 https://www.chictr.org.cn/showprojEN.html?proj=63800.

摘要

背景

阿尔茨海默病(AD)是一种常见的神经系统退行性疾病,对患者及其家庭的生活质量有严重影响。随着人口老龄化,AD已成为中国乃至全球的一个重大公共卫生问题。然而,AD的生理和病理机制尚未完全阐明,且缺乏有效的预防和临床治疗方法。许多研究发现,中药对AD患者的认知功能有良好的治疗效果。补肾开窍方(BSKQF)就是一种用于治疗AD的中药制剂。我们设计了一项关于BSKQF联合盐酸多奈哌齐(DH)治疗AD的真实世界临床研究方案,以评估该方法治疗AD患者的疗效和安全性。

方法

这是一项真实世界、多中心、前瞻性、观察性队列研究方案。该研究将从中国四家医院招募860例AD患者。将同等数量的患者分为接受BSKQF联合DH治疗组或仅接受DH治疗组。分组标准主要基于患者的偏好。疗效指标包括简易精神状态检查表(MMSE)和蒙特利尔认知评估量表(MOCA)得分,将在基线时以及入组后1、2和3个月记录。还将在基线和治疗3个月后通过酶联免疫吸附测定法(ELISA)测量参与研究患者的血浆β淀粉样蛋白42(Aβ42)和血浆微管相关蛋白tau(Tau)水平。将监测并记录参与研究患者的安全性指标和不良事件(AE)。

讨论

本研究将评估BSKQF治疗AD的临床疗效和安全性。研究结果将为BSKQF在AD治疗中的临床应用提供可靠证据。

研究注册

试验注册:中国临床试验注册中心,注册号:ChiCTR2000039670,于2020年11月5日注册,网址:https://www.chictr.org.cn/showprojEN.html?proj=63800

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验