Treatment of Shengqingtongqiao Decoction for mild cognitive impairment of white matter lesions study protocol for a randomized, double-blind, double-dummy, parallel controlled trial.

IF 3.3 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE BMC Complementary Medicine and Therapies Pub Date : 2024-10-11 DOI:10.1186/s12906-024-04654-4
XueYi Han, JieQing Zhang, ZiJun Wei, JiaNing Mei, Xie Long, XiaoMin Zhen, YueChan Zhang, YunYun Zhang
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Abstract

Background: White matter lesions(WML) is an important cause of mild cognitive impairment(MCI). Ginkgo biloba extracts (GBTs) are widely used to treat cognitive dysfunctions. But the treatment of MCI is still limited. Shenqingtongqiao Decoction(SQTQD), as a clinical empirical formula, has received good feedback in treating MCI of WML. However, there was a lack of solid clinical research on SQTQD in treating MCI. The purpose of this study is to evaluate the efficacy of SQTQD in the MCI patients of WML.

Methods: This is a randomized, double-blind, double-dummy, parallel-controlled trial. 80 participants will be assigned to receive SQTQD granules plus GBTs mimetics or SQTQD mimetic granules plus GBTs in a 1:1 ratio. The trial will last 24 weeks, including a 12-week intervention and 12-week follow-up. The primary outcome is MoCA and AVLT. The secondary outcome is a neuropsychological battery (including MMSE, SCWT, TMT, DST, SDMT, BNT, VFT, and CDT), quality of life(BI, ADL, and FAQ scores), emotion assessment(PHQ-9, GAD-7 score) , Fazekas and ARWMCs scale, and fMRI. Researchers will record any adverse events throughout the trial.

Discussion: This study will provide evidence to evaluate the efficacy and safety of SQTQD for MCI of WML compared with GBTs.

Trial registration: The trial is registered at Chinese Clinical Trial Registry: Chinese Clinical Trial Registry (Number: ChiCTR2300068552).

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圣清通窍汤治疗轻度认知障碍白质病变的随机、双盲、双剂、平行对照试验研究方案。
背景:白质病变(WML)是导致轻度认知障碍(MCI)的一个重要原因。银杏叶提取物(GBTs)被广泛用于治疗认知功能障碍。但是,银杏叶提取物对MCI的治疗效果仍然有限。神清通窍汤(SQTQD)作为临床经验方,在治疗WML的MCI方面获得了良好的反馈。然而,关于神清通窍汤治疗 MCI 的临床研究还很缺乏。本研究旨在评估 SQTQD 对 WML MCI 患者的疗效:这是一项随机、双盲、双假、平行对照试验。80名参与者将按1:1的比例被分配接受SQTQD颗粒加GBTs模拟物或SQTQD模拟颗粒加GBTs。试验将持续 24 周,包括 12 周的干预和 12 周的随访。主要结果是MoCA和AVLT。次要结果是神经心理测试(包括 MMSE、SCWT、TMT、DST、SDMT、BNT、VFT 和 CDT)、生活质量(BI、ADL 和 FAQ 评分)、情绪评估(PHQ-9、GAD-7 评分)、Fazekas 和 ARWMCs 量表以及 fMRI。研究人员将在整个试验过程中记录任何不良事件:本研究将为评估SQTQD治疗WML MCI与GBT相比的疗效和安全性提供证据:本试验已在中国临床试验注册中心注册:中国临床试验注册中心(编号:ChiCTR2300068552)。
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来源期刊
BMC Complementary Medicine and Therapies
BMC Complementary Medicine and Therapies INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
6.10
自引率
2.60%
发文量
300
审稿时长
19 weeks
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