Efficacy and safety of Qiangli Dingxuan tablet combined with amlodipine besylate for essential hypertension: a randomized, double-blind, placebo-controlled, parallel-group, multicenter trial

被引:2
|
作者
Lin, Jianguo [1 ,2 ]
Wang, Qingqing [1 ]
Zhong, Dongsheng [1 ]
Zhang, Jinju [1 ]
Yuan, Tianhui [3 ]
Wu, Hui [3 ]
Li, Bin [4 ]
Li, Shuangdi [5 ]
Xie, Xiaoliu [6 ]
An, Dongqing [6 ]
Deng, Yue [5 ]
Xian, Shaoxiang [3 ]
Xiong, Xingjiang [1 ]
Yao, Kuiwu [1 ,7 ]
机构
[1] China Acad Chinese Med Sci, Guanganmen Hosp, Beijing, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Tianjin, Peoples R China
[3] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Guangzhou, Peoples R China
[4] Henan Univ Chinese Med, Affiliated Hosp 1, Zhengzhou, Peoples R China
[5] Changchun Univ Chinese Med, Affiliated Hosp, Changchun, Peoples R China
[6] Tradit Chinese Med Hosp Xinjiang Uygur Autonomous, Urumqi, Peoples R China
[7] China Acad Chinese Med Sci, Eye Hosp, Beijing, Peoples R China
关键词
traditional Chinese medicine; Qiangli Dingxuan tablet; hypertension; randomized controlled trial; classic herbal formula; integrated traditional Chinese and western medicine; CHINESE HERBAL FORMULA; MILLION ADULTS; PREVALENCE;
D O I
10.3389/fphar.2023.1225529
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Hypertension, a major cardiovascular risk factor, severely impacts patients' quality of life. Qiangli Dingxuan tablet (QDT) is a formally approved Chinese patent medicine, which has been widely used as an adjunctive treatment for hypertension. This study aimed to investigate the antihypertensive efficacy and safety of QDT combined with amlodipine besylate in patients with essential hypertension.Methods: In this randomized, double-blind, placebo-controlled, parallel-group, multicenter trial conducted in China, patients diagnosed with grade 1 to 2 essential hypertension were randomly assigned in a 1:1 to the treatment of QDT or placebo for 12 weeks, alongside their ongoing treatment with amlodipine besylate. The primary outcome was the change in office blood pressure (BP) from baseline to 12 weeks. In addition, safety analysis included the assessment of vital signs and laboratory values.Results: At baseline, 269 patients were randomly assigned to the QDT group (n = 133) or the placebo group (n = 136), and there were no significant differences in baseline characteristics between the two groups. The primary outcome based on the full analysis set from baseline to 12 weeks showed that the mean difference in the change of office systolic BP reduction between the two groups was 6.86 mmHg (95%CI, 4.84 to 8.88, p < 0.0001), for office diastolic BP, the mean difference in the change of office diastolic BP reduction between the two groups was 4.64 mmHg (95%CI, 3.10 to 6.18, p < 0.0001). In addition, traditional Chinese medicine symptom scores were significantly decreased in the QDT group compared with the placebo group. No severe adverse events attributable to QDT were reported.Conclusion: The combination of QDT and amlodipine besylate demonstrates superior efficacy compared to amlodipine besylate monotherapy in the management of essential hypertension. QDT shows potential as an adjunctive treatment for essential hypertension. However, further rigorous clinical trials are warranted to validate these findings.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] A randomized, double-blind, placebo-controlled, parallel-group, multicenter trial of four doses of tasosartan in patients with essential hypertension
    Lacourcière, Y
    Pool, JL
    Svetkey, L
    Gradman, AH
    Larochelle, P
    de Champlain, J
    Smith, WB
    AMERICAN JOURNAL OF HYPERTENSION, 1998, 11 (04) : 454 - 461
  • [2] Efficacy and Safety of Allisartan Isoproxil/Amlodipine in Patients With Essential Hypertension Uncontrolled by Amlodipine: A Phase III, Multicenter, Double-Blind, Parallel-Group, Randomized Controlled Trial
    Chi, Hongjie
    Zhang, Xin
    Ma, Shumei
    Pan, Gang
    Lian, Xiaojuan
    Chen, Yan
    Pei, Haotian
    Liu, Zichen
    Lin, Xiangmin
    JOURNAL OF CLINICAL HYPERTENSION, 2025, 27 (01):
  • [3] Multicenter, randomized, double-blind, placebo-controlled, parallel trial comparing the safety and efficacy of rufinamide
    Biton, V
    Rosenfeld, W
    Schachter, S
    Perdomo, C
    Arroyo, S
    ANNALS OF NEUROLOGY, 2005, 58 : S114 - S114
  • [4] The efficacy and safety of 'antianxiety granule' for anxiety disorder: a multicentre, randomized, double-blind, placebo-controlled, parallel-group trial
    Sha, Zhongwei
    Hou, Yiping
    Xue, Chunchun
    Li, Ou
    Li, Zhimin
    Wang, Huiru
    Zhang, Wenjing
    Xu, Jian
    TRIALS, 2020, 21 (01)
  • [5] The efficacy and safety of 'antianxiety granule' for anxiety disorder: a multicentre, randomized, double-blind, placebo-controlled, parallel-group trial
    Zhongwei Sha
    Yiping Hou
    Chunchun Xue
    Ou Li
    Zhimin Li
    Huiru Wang
    Wenjing Zhang
    Jian Xu
    Trials, 21
  • [6] A randomized, double-blind, parallel-group, placebo-controlled Phase 3 trial to evaluate efficacy and safety of ocrelizumab in PPMS
    Montalban, Xavier
    Hemmer, Bernhard
    Rammohan, Kottil W.
    Giovannoni, Gavin
    De Seze, Jerome
    Bar-Or, Amit
    Arnold, Douglas L.
    Sauter, Annette
    Masterman, Donna
    Fontoura, Paulo
    Chin, Peter
    Garren, Hideki
    Wolinsky, Jerry S.
    MULTIPLE SCLEROSIS JOURNAL, 2016, 22 : 17 - 17
  • [7] Efficacy and safety of fremanezumab for episodic migraine prevention: Multicenter, randomized, double-blind, placebo-controlled, parallel-group trial in Japanese and Korean patients
    Sakai, Fumihiko
    Suzuki, Norihiro
    Kim, Byung-Kun
    Tatsuoka, Yoshihisa
    Imai, Noboru
    Ning, Xiaoping
    Ishida, Miki
    Nagano, Kaori
    Iba, Katsuhiro
    Kondo, Hiroyuki
    Koga, Nobuyuki
    HEADACHE, 2021, 61 (07): : 1102 - 1111
  • [8] Efficacy and safety of fremanezumab for chronic migraine prevention: Multicenter, randomized, double-blind, placebo-controlled, parallel-group trial in Japanese and Korean patients
    Sakai, Fumihiko
    Suzuki, Norihiro
    Kim, Byung-Kun
    Igarashi, Hisaka
    Hirata, Koichi
    Takeshima, Takao
    Ning, Xiaoping
    Shima, Tomoko
    Ishida, Miki
    Iba, Katsuhiro
    Kondo, Hiroyuki
    Koga, Nobuyuki
    HEADACHE, 2021, 61 (07): : 1092 - 1101
  • [9] The Efficacy and Safety of Wenxin Keli in Patients with Frequent Premature Ventricular Contractions: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Trial
    Hua, Wei
    Gao, Run-Lin
    Zhao, Bu-Chang
    Wang, Jing
    Chen, Xu-Hua
    Cai, Chi
    Zhang, Shu
    CHINESE MEDICAL JOURNAL, 2015, 128 (19) : 2557 - 2564
  • [10] Comparison of efficacy and tolerability of amlodipine orotate versus amlodipine besylate in adult patients with mild to moderate hypertension: A multicenter, randomized, double-blind, placebo-controlled, parallel-group, 8-week follow-up, noninferiority trial
    Hong, Soon Jun
    Ahn, Tae-Hoon
    Baek, Sang-Hong
    Cho, Wook-Hyun
    Jeon, Hyee-Kyoung
    Kyun, Jun
    Yoon, Myeong Ho
    Lee, Kwan Jeh
    Lim, Do-Sun
    CLINICAL THERAPEUTICS, 2006, 28 (04) : 537 - 551