Randomised clinical trial: Efficacy and safety of Qing-Chang-Hua-Shi granules in a multicenter, randomized, and double-blind clinical trial of patients with moderately active ulcerative colitis

被引:21
作者
Shen, Hong [1 ]
Zhang, Shengsheng [2 ]
Zhao, Wenxia [3 ]
Ren, Shunping [4 ]
Ke, Xiao [5 ]
Gu, Qinghua [6 ]
Tang, Zhipeng [7 ]
Xie, Jingri [8 ]
Chen, Suning [9 ]
Chen, Yan [10 ]
Zou, Jiandong [1 ]
Zhang, Lu [1 ]
Shen, Zhaofeng [1 ]
Zheng, Kai [1 ]
Liu, Yajun [1 ]
Gu, Peiqing [1 ]
Cheng, Jiafei [1 ]
Hu, Jingyi [1 ]
Zhu, Lei [1 ]
机构
[1] Nanjing Univ Chinese Med, Affiliated Hosp, Jiangsu Prov Hosp Chinese Med, Nanjing 210029, Peoples R China
[2] Beijing Hosp Tradit Chinese Med, Beijing, Peoples R China
[3] Henan Univ CM, Affiliated Hosp 1, Zhengzhou, Peoples R China
[4] Hosp Shanxi Univ Chinese Med, Taiyuan, Peoples R China
[5] Fujian Tradit Chinese Med Univ, Affiliated Hosp 2, Fuzhou, Peoples R China
[6] Nantong Hosp Tradit Chinese Med, Nantong, Peoples R China
[7] Shanghai Univ Tradit Chinese Med, LongHua Hosp, Shanghai, Peoples R China
[8] Heilongjiang Univ Chinese Med, Affiliated Hosp 1, Haerbin, Peoples R China
[9] China Med Univ, Shengjing Hosp, Shenyang, Peoples R China
[10] GuangDong Prov Hosp Chinese Med, Guangzhou, Peoples R China
关键词
Qing-Chang-Hua-Shi (QCHS); Clinical trial; Ulcerative colitis; Inflammatory bowel disease; Mesalazine; INFLAMMATORY-BOWEL-DISEASE; EXTRACT HMPL-004; MANAGEMENT; MESALAMINE; REMISSION; THERAPY; MESALAZINE; IBD;
D O I
10.1016/j.biopha.2021.111580
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Qing-Chang-Hua-Shi (QCHS) is a Chinese herbal formula, which is composed of 11 herbs. Studies have also shown that QCHS granules can alleviate colitis in animal models by preventing inflammatory responses and suppressing apoptosis through the MEK/ERK signaling pathway. To determine the efficacy and safety of QCHS granules in patients with moderately active UC. We performed a multicenter, randomized, placebo-controlled, double-blind study of patients with moderately active UC who did not respond to 4 weeks of mesalazine therapy at the maximum dose. Patients were randomly assigned to groups and administered QCHS granules (125 g/ day, n = 59) or an identical placebo, which was similar to the QCHS granules in color and taste (125 g/day, n = 60), with continued 5-ASA 4 g/d therapy for 12 weeks. The primary outcome was the rate of clinical response and clinical remission at week 12. The secondary outcomes were health-related quality of life, endoscopic response rate, and mucosal healing rate. Any changes in mucus/bloody stool and diarrhea were recorded. Out of the 119 enrolled patients at 10 different centers in China, 102 patients completed the trial. Clinical remission and clinical response were seen in 31.48% and 92.59% of QCHS-treated patients, and 12.50% and 72.92% of placebotreated patients, respectively. There was a significant difference between the two treatment groups. More patients receiving QCHS granules vs. placebo achieved remission of mucus/bloody stool (70.37% vs. 47.92%, P = 0.0361). Adverse event rates were similar (QCHS granules 38.33%; placebo 25.42%). In conclusion, QCHS granules were superior to the placebo in introducing clinical remission and mucosal healing, as well as in relieving mucus/blood stool in patients with moderately active and 5-ASA-refractory UC.
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页数:8
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