Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial

Objective. In the 24-week randomized, double-blind, double-placebo, parallel-controlled trial, we aimed to test the effects of herbal therapy with amnestic mild cognitive impairment (aMCI). Methods. A total of 324 patients with aMCI entered a 2-week placebo run-in period followed by 24 weeks’ treatm...

Full description

Bibliographic Details
Main Authors: Jinzhou Tian, Jing Shi, Tao Li, Lin Li, Zhiliang Wang, Xiaobin Li, Zhu Lv, Qingshan Zheng, Mingqing Wei, Yongyan Wang
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Evidence-Based Complementary and Alternative Medicine
Online Access:http://dx.doi.org/10.1155/2017/4251747
id doaj-74c0d47444b14445b4592634e7cd21a2
record_format Article
spelling doaj-74c0d47444b14445b4592634e7cd21a22020-11-24T22:29:49ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882017-01-01201710.1155/2017/42517474251747Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III TrialJinzhou Tian0Jing Shi1Tao Li2Lin Li3Zhiliang Wang4Xiaobin Li5Zhu Lv6Qingshan Zheng7Mingqing Wei8Yongyan Wang9Third Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, ChinaThird Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, ChinaDepartment of Neurology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaLaboratory of Pharmacy, Xuanwu Hospital, Capital University of Medical Sciences, Beijing 100053, ChinaNorth China Pharmaceutical Group Corporation, Hebei 050015, ChinaNorth China Pharmaceutical Group Corporation, Hebei 050015, ChinaNorth China Pharmaceutical Group Corporation, Hebei 050015, ChinaDrug Clinical Trial Centre, Shanghai University of Chinese Medicine, Shanghai 200032, ChinaThird Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, ChinaInstitute of Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, ChinaObjective. In the 24-week randomized, double-blind, double-placebo, parallel-controlled trial, we aimed to test the effects of herbal therapy with amnestic mild cognitive impairment (aMCI). Methods. A total of 324 patients with aMCI entered a 2-week placebo run-in period followed by 24 weeks’ treatment of either (a) herbal capsule (5 shenwu capsules/administration, 3 times/day) and placebo identical to donepezil tablets (n=216) or (b) donepezil (5 mg/day) and placebo identical to herbal capsule (n=108). Results. Herbal therapy showed a significant improvement on the primary efficacy measure, measured by Alzheimer Disease Assessment Scale-cognitive subscale (ADAS-cog), and showed a mean decrease from baseline of 4.23 points at the endpoint, without a significant difference from the donepezil group. Secondary efficacy measurement of the Logical Memory II Delayed Story Recall subtest (DSR) showed modest improvement in those taking herbal capsule compared to baseline, and there was no significant difference from donepezil group. The frequency of adverse events was much less in the herbal therapy group than the donepezil. Conclusion. Herbal therapy demonstrated a significant improvement in cognition and memory, which were similar to the donepezil in patients with aMCI. Herbal therapy was safe and well tolerated. Trial Registration. This study is registered with clinicaltrials.gov NCT01451749.http://dx.doi.org/10.1155/2017/4251747
collection DOAJ
language English
format Article
sources DOAJ
author Jinzhou Tian
Jing Shi
Tao Li
Lin Li
Zhiliang Wang
Xiaobin Li
Zhu Lv
Qingshan Zheng
Mingqing Wei
Yongyan Wang
spellingShingle Jinzhou Tian
Jing Shi
Tao Li
Lin Li
Zhiliang Wang
Xiaobin Li
Zhu Lv
Qingshan Zheng
Mingqing Wei
Yongyan Wang
Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
Evidence-Based Complementary and Alternative Medicine
author_facet Jinzhou Tian
Jing Shi
Tao Li
Lin Li
Zhiliang Wang
Xiaobin Li
Zhu Lv
Qingshan Zheng
Mingqing Wei
Yongyan Wang
author_sort Jinzhou Tian
title Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
title_short Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
title_full Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
title_fullStr Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
title_full_unstemmed Efficacy and Safety of an Herbal Therapy in Patients with Amnestic Mild Cognitive Impairment: A 24-Week Randomized Phase III Trial
title_sort efficacy and safety of an herbal therapy in patients with amnestic mild cognitive impairment: a 24-week randomized phase iii trial
publisher Hindawi Limited
series Evidence-Based Complementary and Alternative Medicine
issn 1741-427X
1741-4288
publishDate 2017-01-01
description Objective. In the 24-week randomized, double-blind, double-placebo, parallel-controlled trial, we aimed to test the effects of herbal therapy with amnestic mild cognitive impairment (aMCI). Methods. A total of 324 patients with aMCI entered a 2-week placebo run-in period followed by 24 weeks’ treatment of either (a) herbal capsule (5 shenwu capsules/administration, 3 times/day) and placebo identical to donepezil tablets (n=216) or (b) donepezil (5 mg/day) and placebo identical to herbal capsule (n=108). Results. Herbal therapy showed a significant improvement on the primary efficacy measure, measured by Alzheimer Disease Assessment Scale-cognitive subscale (ADAS-cog), and showed a mean decrease from baseline of 4.23 points at the endpoint, without a significant difference from the donepezil group. Secondary efficacy measurement of the Logical Memory II Delayed Story Recall subtest (DSR) showed modest improvement in those taking herbal capsule compared to baseline, and there was no significant difference from donepezil group. The frequency of adverse events was much less in the herbal therapy group than the donepezil. Conclusion. Herbal therapy demonstrated a significant improvement in cognition and memory, which were similar to the donepezil in patients with aMCI. Herbal therapy was safe and well tolerated. Trial Registration. This study is registered with clinicaltrials.gov NCT01451749.
url http://dx.doi.org/10.1155/2017/4251747
work_keys_str_mv AT jinzhoutian efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT jingshi efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT taoli efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT linli efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT zhiliangwang efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT xiaobinli efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT zhulv efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT qingshanzheng efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT mingqingwei efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
AT yongyanwang efficacyandsafetyofanherbaltherapyinpatientswithamnesticmildcognitiveimpairmenta24weekrandomizedphaseiiitrial
_version_ 1725742964500594688