Comparative Evaluation of Effectiveness of Standard of Care Alone and in Combination With Homoeopathic Treatment in COVID-19-Related Rhino-Orbito-Cerebral Mucormycosis (ROCM): Protocol for a Single Blind, Randomized Controlled Trial.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Research Protocols Pub Date : 2025-03-19 DOI:10.2196/57905
Harleen Kaur, Jyoti Sachdeva, Ramesh Bawaskar, Twinkle Goyal
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Abstract

Background: Rhino-orbital-cerebral mucormycosis (ROCM) is the most common (45%-74%) mucormycosis in India. With contemporary medical care, ROCM has a mortality rate of 40%-50% and 70% of survivors are left with residual defects. Recently, several cases of mucormycosis in people with COVID-19 have been increasingly reported worldwide, from India, due to immune dysregulation caused by SARS-CoV-2. To reduce the high mortality rate and residual defect in most survivors under the guidelines of the Ministry of AYUSH, the Government of India recommended homoeopathy as an add-on therapy to maximize the effectiveness of standard treatment in conventional therapy.

Objective: This study aimed to evaluate the role of existing homoeopathic treatment as an adjuvant therapy in patients with COVID-19-related ROCM and enhancing the survival of the patients hospitalized due to COVID-19 infection and to access the initial treatment response and duration required for significant or complete recovery in patients receiving adjuvant treatment.

Methods: This superiority, randomized controlled clinical trial would include two parallel comparator groups A and B. Group A would be the experimental group and would receive homoeopathic treatment along with the standard line of treatment as per investigational medicinal product (IMP) and group B would be the control arm and would receive standard line of treatment as per IMP along with identical placebo. Allocation would be 1:1 through randomization. Based on the inclusion and exclusion criteria, 36 participants per arm would be screened. Participants would be assessed clinically twice a day and magnetic resonance imagery or endoscopy cum-biopsy would be assessed on days 1, 14, and 28. Laboratory investigations may vary as per demand of disease conditions.

Results: In India, the COVID-19 pandemic, particularly during the second wave, resulted in a surge of mucormycosis cases among patients with COVID-19. At the time this protocol was being developed, there was a significant spike in mucormycosis cases in India, particularly in Mumbai (June 2021). However, by the time the Central Council for Research in Homoeopathy obtained the necessary approvals and ethical clearance for the study, the incidence of mucormycosis had drastically declined (September 2021). As a result, the study was not initiated and registered. The authors feel it is their ethical responsibility to share the reviewed protocol with the medical community as a reference for future work.

Conclusions: This study aims to evaluate the role of existing homoeopathic medicines as an adjuvant therapy in managing COVID-19-related ROCM, potentially contributing to the use of homoeopathy as an evidence-based medical approach. The protocol can also serve as a valuable resource for clinicians and researchers addressing mucormycosis cases unrelated to COVID-19, particularly in immunocompromised patients. It would help ensure preparedness, whether or not sufficient evidence is available, in the event of a future health emergency.

International registered report identifier (irrid): PRR1-10.2196/57905.

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单独标准护理与联合顺势疗法治疗covid -19相关鼻-眶-脑毛霉菌病(ROCM)疗效的比较评价:单盲、随机对照试验方案
背景:鼻-眶-脑毛霉菌病(ROCM)是印度最常见的(45%-74%)毛霉菌病。在现代医疗条件下,ROCM的死亡率为40%-50%,70%的幸存者留下了残留的缺陷。最近,由于SARS-CoV-2引起的免疫失调,世界各地越来越多地报告了来自印度的几例COVID-19患者的毛霉菌病病例。为了降低大多数幸存者的高死亡率和残留缺陷,印度政府建议将顺势疗法作为一种附加疗法,以最大限度地提高常规疗法中标准治疗的有效性。目的:本研究旨在评估现有顺势疗法作为辅助治疗在COVID-19相关ROCM患者中的作用,提高因COVID-19感染住院患者的生存率,并了解接受辅助治疗的患者显著或完全康复所需的初始治疗反应和持续时间。方法:这项优势的随机对照临床试验将包括两个平行的比较组A和B。A组将作为实验组,按照研究药物(IMP)的标准路线接受顺势疗法治疗,B组将作为对照组,按照研究药物(IMP)的标准路线接受治疗,同时接受相同的安慰剂。通过随机化,分配比例为1:1。根据纳入和排除标准,每组36名受试者将被筛选。参与者将每天进行两次临床评估,并在第1、14和28天进行磁共振成像或内窥镜和活检评估。实验室调查可根据疾病条件的要求而有所不同。结果:在印度,COVID-19大流行,特别是在第二波疫情期间,导致COVID-19患者中毛霉病病例激增。在制定该议定书时,印度,特别是孟买(2021年6月)的毛霉病病例显著增加。然而,当顺势疗法研究中央委员会为该研究获得必要的批准和伦理许可时,毛霉病的发病率急剧下降(2021年9月)。因此,这项研究没有发起和登记。作者认为与医学界分享审查后的方案作为今后工作的参考是他们的道德责任。结论:本研究旨在评估现有顺势疗法药物作为辅助疗法在管理covid -19相关ROCM中的作用,可能有助于顺势疗法作为循证医学方法的使用。该方案还可作为临床医生和研究人员处理与COVID-19无关的毛霉病病例的宝贵资源,特别是在免疫功能低下患者中。这将有助于确保在未来发生突发卫生事件时做好准备,无论是否有足够的证据。国际注册报告标识符(irrid): PRR1-10.2196/57905。
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