Meta-Analysis of Randomized, Double Blind, Controlled Studies Confirms the Efficacy and Safety of Esberitox in the Treatment of the Common Cold

B. Naser, J. Schnitker, C. Hentschel, Jennifer-Christin Kuchernig, A. Holtdirk, G. Schöneberg, P. Nicken, K. Nolte, H. Henneicke-von Zepelin
{"title":"Meta-Analysis of Randomized, Double Blind, Controlled Studies Confirms the Efficacy and Safety of Esberitox in the Treatment of the Common Cold","authors":"B. Naser, J. Schnitker, C. Hentschel, Jennifer-Christin Kuchernig, A. Holtdirk, G. Schöneberg, P. Nicken, K. Nolte, H. Henneicke-von Zepelin","doi":"10.12970/2308-8044.2021.09.04","DOIUrl":null,"url":null,"abstract":"Herbal medicines like Esberitox (TOX, wild indigo root stock, echinacea root, thuja tips and leaves) are used to treat common colds. Several randomized, controlled trials (RCT) document the efficacy and safety of TOX in this indication. So far its efficacy and safety has not been evaluated meta-analytically. \nWe included individual patient data from all 825 patients from 3 RCTs. 693 patients had been treated with TOX, 132 with placebo (PLA) (7-9 days). All symptom scores were adjusted to baseline and meta-analyzed regarding area under the curve (AUC), time to response (≥50% decrease of symptom score), response rate and duration of the cold. \nThe AUCs of the rhinitis score were 19.05 with TOX superior to 20.57 with PLA (p=0.020), bronchitis score 14.92 versus 16.16 (p=0.039) and well-being 208.4 versus 216.4 (p=0.008). Response rates were higher in TOX than PLA in all scores. The times to response showed an acceleration of the healing process of rhinitis (1.5 days, p=0.049), bronchitis (2 days) and pain (2 days, p=0.008). The duration of the cold was shortened by TOX by up to 2.3 days. The ADR-rate did not differ significantly (2.7% vs. 1.5%, p=0.41). Tolerability was good to very good in 98.4% (TOX) and 99.2% (PLA) (p=0.34). In conclusion, this meta-analysis confirmed the efficacy and tolerability of Esberitox at a higher level of evidence. It accelerates the improvement of cold symptoms by up to 2 days and shortens the duration of colds by up to 2.3 days.","PeriodicalId":307164,"journal":{"name":"Journal of Modern Medicinal Chemistry","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Modern Medicinal Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12970/2308-8044.2021.09.04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Herbal medicines like Esberitox (TOX, wild indigo root stock, echinacea root, thuja tips and leaves) are used to treat common colds. Several randomized, controlled trials (RCT) document the efficacy and safety of TOX in this indication. So far its efficacy and safety has not been evaluated meta-analytically. We included individual patient data from all 825 patients from 3 RCTs. 693 patients had been treated with TOX, 132 with placebo (PLA) (7-9 days). All symptom scores were adjusted to baseline and meta-analyzed regarding area under the curve (AUC), time to response (≥50% decrease of symptom score), response rate and duration of the cold. The AUCs of the rhinitis score were 19.05 with TOX superior to 20.57 with PLA (p=0.020), bronchitis score 14.92 versus 16.16 (p=0.039) and well-being 208.4 versus 216.4 (p=0.008). Response rates were higher in TOX than PLA in all scores. The times to response showed an acceleration of the healing process of rhinitis (1.5 days, p=0.049), bronchitis (2 days) and pain (2 days, p=0.008). The duration of the cold was shortened by TOX by up to 2.3 days. The ADR-rate did not differ significantly (2.7% vs. 1.5%, p=0.41). Tolerability was good to very good in 98.4% (TOX) and 99.2% (PLA) (p=0.34). In conclusion, this meta-analysis confirmed the efficacy and tolerability of Esberitox at a higher level of evidence. It accelerates the improvement of cold symptoms by up to 2 days and shortens the duration of colds by up to 2.3 days.
随机、双盲、对照研究的荟萃分析证实了埃斯贝里托克斯治疗普通感冒的有效性和安全性
像Esberitox这样的草药(TOX,野生靛蓝根,紫锥菊根,土树叶)被用来治疗普通感冒。几项随机对照试验(RCT)证明了TOX在这一适应症中的有效性和安全性。到目前为止,其有效性和安全性尚未进行meta分析评价。我们纳入了来自3个随机对照试验的所有825例患者的个体患者数据。693例患者接受TOX治疗,132例患者接受安慰剂(PLA)治疗(7-9天)。将所有症状评分调整至基线,并对曲线下面积(AUC)、反应时间(症状评分下降≥50%)、反应率和感冒持续时间进行meta分析。鼻炎评分为19.05,TOX优于PLA评分为20.57 (p=0.020),支气管炎评分为14.92比16.16 (p=0.039),幸福感评分为208.4比216.4 (p=0.008)。TOX组的有效率高于PLA组。反应时间显示鼻炎(1.5天,p=0.049)、支气管炎(2天)和疼痛(2天,p=0.008)的愈合过程加快。由于TOX的作用,感冒的持续时间缩短了2.3天。不良反应发生率无显著差异(2.7% vs. 1.5%, p=0.41)。98.4% (TOX)和99.2% (PLA)的耐受性好至极好(p=0.34)。总之,这项荟萃分析在更高的证据水平上证实了Esberitox的疗效和耐受性。它能将感冒症状的改善加速2天,并将感冒的持续时间缩短2.3天。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信