Kaur Harleen, Sachdeva Jyoti, Bawaskar Ramesh, Goyal Twinkle
Central Council for Research in Homeopathy, New Delhi, India.
Dr.D.P. Rastogi Central Research Institute Homeopathy, Noida, India.
JMIR Res Protoc. 2025 Mar 19;14:e57905. doi: 10.2196/57905.
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.
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.
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.
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.
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.
鼻眶脑型毛霉菌病(ROCM)是印度最常见的毛霉菌病(占45%-74%)。在当代医疗条件下,ROCM的死亡率为40%-50%,70%的幸存者会留下残余缺陷。最近,全球范围内(包括印度)越来越多地报道了新冠病毒感染患者中出现的几例毛霉菌病病例,这是由SARS-CoV-2引起的免疫失调所致。为了在阿育吠陀部的指导方针下降低大多数幸存者的高死亡率和残余缺陷,印度政府推荐顺势疗法作为辅助疗法,以最大限度地提高传统疗法中标准治疗的效果。
本研究旨在评估现有顺势疗法作为辅助疗法在新冠病毒相关ROCM患者中的作用,提高因新冠病毒感染住院患者的生存率,并了解接受辅助治疗的患者实现显著或完全康复所需的初始治疗反应和时间。
这项优效性随机对照临床试验将包括两个平行的比较组A和B。A组为试验组,将根据试验用药品(IMP)接受顺势疗法治疗以及标准治疗方案;B组为对照组,将根据IMP接受标准治疗方案以及相同的安慰剂。通过随机化进行1:1分配。根据纳入和排除标准,每组将筛选36名参与者。参与者将每天进行两次临床评估,并在第1天、第14天和第28天进行磁共振成像或内镜活检。实验室检查可能会根据疾病情况的需求而有所不同。
在印度,新冠疫情,尤其是在第二波疫情期间,导致新冠病毒感染患者中的毛霉菌病病例激增。在制定本方案时,印度的毛霉菌病病例大幅增加,特别是在孟买(2021年6月)。然而,当顺势疗法中央研究委员会获得该研究的必要批准和伦理许可时,毛霉菌病的发病率已大幅下降(2021年9月)。因此,该研究未启动和注册。作者认为,与医学界分享经过审核的方案是他们的道德责任,可为未来的工作提供参考。
本研究旨在评估现有顺势疗法药物作为辅助疗法在治疗新冠病毒相关ROCM中的作用,可能有助于将顺势疗法作为一种循证医学方法来使用。该方案也可为处理与新冠病毒无关的毛霉菌病病例的临床医生和研究人员提供宝贵资源,特别是在免疫功能低下的患者中。无论是否有足够的证据,它都将有助于在未来发生健康紧急情况时做好准备。
国际注册报告识别码(IRRID):PRR1-10.2196/57905。