Homeopathy as an Adjuvant to Standard Care in Moderate and Severe Cases of COVID-19: A Single-Blind, Randomized, Placebo-Controlled Study.

IF 1.2 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE
Homeopathy Pub Date : 2023-08-01 DOI:10.1055/s-0042-1755365
Harleen Kaur, Subhash Kaushik, Gurpreet Singh, Arvind Kumar, Shweta Singh, Tania Chatterjee, Syed Ali, Khushbu Gautam, Maneet Parewa, Naval Kumar Verma, Sushma Bhatnagar, Suraj Pal Singh, Varun Shekhar, Anil Khurana
{"title":"Homeopathy as an Adjuvant to Standard Care in Moderate and Severe Cases of COVID-19: A Single-Blind, Randomized, Placebo-Controlled Study.","authors":"Harleen Kaur,&nbsp;Subhash Kaushik,&nbsp;Gurpreet Singh,&nbsp;Arvind Kumar,&nbsp;Shweta Singh,&nbsp;Tania Chatterjee,&nbsp;Syed Ali,&nbsp;Khushbu Gautam,&nbsp;Maneet Parewa,&nbsp;Naval Kumar Verma,&nbsp;Sushma Bhatnagar,&nbsp;Suraj Pal Singh,&nbsp;Varun Shekhar,&nbsp;Anil Khurana","doi":"10.1055/s-0042-1755365","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to evaluate whether individualized homeopathic medicines have a greater adjunctive effect than adjunctive placebos in the treatment of moderate and severe cases of coronavirus disease 2019 (COVID-19).</p><p><strong>Methods: </strong>The study was a randomized, single-blind, prospective, placebo-controlled clinical trial set in the clinical context of standard care.</p><p><strong>Intervention: </strong>Patients of either sex, admitted in a tertiary care hospital, suffering from moderate or severe COVID-19 and above 18 years of age were included. In total, 150 patients were recruited and then randomly divided into two groups to receive either individualized homeopathic medicines or placebos, in addition to the standard treatment of COVID-19.</p><p><strong>Outcome measures: </strong>The primary outcome was time taken to achieve RT-PCR-confirmed virus clearance for COVID-19. Secondary outcomes were changes in the Clinical Ordinal Outcomes Scale (COOS) of the World Health Organization, the patient-reported MYMOP2 scale, and several biochemical parameters. Parametric data were analyzed using unpaired <i>t</i>-test. Non-parametric data were analyzed using the Wilcoxon signed rank test. Categorical data were analyzed using Chi-square test.</p><p><strong>Results: </strong>In total, 72 participants of the add-on homeopathy (AoH) group showed conversion of RT-PCR status to negative, in an average time of 7.53 ± 4.76 days (mean ± SD), as compared with 11.65 ± 9.54 days in the add-on placebo (AoP) group (<i>p</i> = 0.001). The mean COOS score decreased from 4.26 ± 0.44 to 3.64 ± 1.50 and from 4.3 ± 0.46 to 4.07 ± 1.8 in the AoH and AoP groups respectively (<i>p</i> = 0.130). The mortality rate for the AoH group was 9.7% compared with 17.3% in the AoP group. The MYMOP2 scores between the two groups differed significantly (<i>p</i> = 0.001), in favor of AoH. Inter-group differences in the pre- and post- mean values of C-reactive protein, fibrinogen, total leukocyte count, platelet count and alkaline phosphatase were each found to be statistically significant (<i>p</i> <0.05), favoring AoH; six other biochemical parameters showed no statistically significant differences.</p><p><strong>Conclusion: </strong>The study suggests homeopathy may be an effective adjunct to standard care for treating moderate and severe COVID-19 patients. More rigorous, including double-blinded, studies should be performed to confirm or refute these initial findings.</p>","PeriodicalId":13227,"journal":{"name":"Homeopathy","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Homeopathy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1055/s-0042-1755365","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INTEGRATIVE & COMPLEMENTARY MEDICINE","Score":null,"Total":0}
引用次数: 3

Abstract

Objectives: This study aimed to evaluate whether individualized homeopathic medicines have a greater adjunctive effect than adjunctive placebos in the treatment of moderate and severe cases of coronavirus disease 2019 (COVID-19).

Methods: The study was a randomized, single-blind, prospective, placebo-controlled clinical trial set in the clinical context of standard care.

Intervention: Patients of either sex, admitted in a tertiary care hospital, suffering from moderate or severe COVID-19 and above 18 years of age were included. In total, 150 patients were recruited and then randomly divided into two groups to receive either individualized homeopathic medicines or placebos, in addition to the standard treatment of COVID-19.

Outcome measures: The primary outcome was time taken to achieve RT-PCR-confirmed virus clearance for COVID-19. Secondary outcomes were changes in the Clinical Ordinal Outcomes Scale (COOS) of the World Health Organization, the patient-reported MYMOP2 scale, and several biochemical parameters. Parametric data were analyzed using unpaired t-test. Non-parametric data were analyzed using the Wilcoxon signed rank test. Categorical data were analyzed using Chi-square test.

Results: In total, 72 participants of the add-on homeopathy (AoH) group showed conversion of RT-PCR status to negative, in an average time of 7.53 ± 4.76 days (mean ± SD), as compared with 11.65 ± 9.54 days in the add-on placebo (AoP) group (p = 0.001). The mean COOS score decreased from 4.26 ± 0.44 to 3.64 ± 1.50 and from 4.3 ± 0.46 to 4.07 ± 1.8 in the AoH and AoP groups respectively (p = 0.130). The mortality rate for the AoH group was 9.7% compared with 17.3% in the AoP group. The MYMOP2 scores between the two groups differed significantly (p = 0.001), in favor of AoH. Inter-group differences in the pre- and post- mean values of C-reactive protein, fibrinogen, total leukocyte count, platelet count and alkaline phosphatase were each found to be statistically significant (p <0.05), favoring AoH; six other biochemical parameters showed no statistically significant differences.

Conclusion: The study suggests homeopathy may be an effective adjunct to standard care for treating moderate and severe COVID-19 patients. More rigorous, including double-blinded, studies should be performed to confirm or refute these initial findings.

顺势疗法作为中重度COVID-19病例标准治疗的辅助:一项单盲、随机、安慰剂对照研究
目的:本研究旨在评估个体化顺势疗法药物在治疗中重度冠状病毒病2019 (COVID-19)时是否比辅助安慰剂具有更大的辅助作用。方法:该研究是一项随机、单盲、前瞻性、安慰剂对照的临床试验,在标准治疗的临床背景下进行。干预措施:纳入在三级保健医院住院、患有中度或重度COVID-19且年龄在18岁以上的男女患者。总共招募了150名患者,然后随机分为两组,除了接受COVID-19的标准治疗外,还接受个性化顺势疗法药物或安慰剂。结局指标:主要结局指标是实现rt - pcr确认的COVID-19病毒清除所需的时间。次要结局是世界卫生组织临床顺序结局量表(COOS)、患者报告的MYMOP2量表和一些生化参数的变化。参数数据采用非配对t检验进行分析。非参数数据采用Wilcoxon符号秩检验进行分析。分类资料采用卡方检验进行分析。结果:共有72名顺势疗法(AoH)组患者的RT-PCR状态转化为阴性,平均时间为7.53±4.76天(平均±SD),而安慰剂(AoP)组为11.65±9.54天(p = 0.001)。AoH组和AoP组的平均COOS评分分别从4.26±0.44分降至3.64±1.50分,从4.3±0.46分降至4.07±1.8分(p = 0.130)。AoH组死亡率为9.7%,AoP组为17.3%。两组间MYMOP2评分差异有统计学意义(p = 0.001), AoH组更有利。c反应蛋白、纤维蛋白原、白细胞总计数、血小板计数和碱性磷酸酶的前后均值组间差异均有统计学意义(p)。结论:顺势疗法可能是治疗中重度COVID-19患者的有效辅助疗法。应该进行更严格的研究,包括双盲研究,以证实或反驳这些初步发现。
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
Homeopathy
Homeopathy 医学-全科医学与补充医学
CiteScore
3.40
自引率
70.60%
发文量
34
审稿时长
20.1 weeks
期刊介绍: Homeopathy is an international peer-reviewed journal aimed at improving the fundamental understanding and clinical practice of homeopathy by publishing relevant high-quality original research articles, reviews, and case reports. It also promotes commentary and debate on matters of topical interest in homeopathy.
×
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