Clinical evaluation of AYUSH-SL in patients receiving mass drug administration for the treatment of chronic inflammatory lymphedema, a double blind, placebo controlled, multicentric study.

IF 0.8 4区 医学 Q4 INFECTIOUS DISEASES Journal of Vector Borne Diseases Pub Date : 2024-12-05 DOI:10.4103/JVBD.JVBD_61_24
Achintya Mitra, Gurucharan Bhuyan, C Muralikrishna, S M Naser, K K Ratha, G Babu, B Venkateswarlu, Sujata Dhoke, Chiranjib Bagchi, Renu Singh, Arunabh Tripathi, Rakesh Rana, B S Sharma, Shruti Khanduri, Bharti Gupta, Bcs Rao, Adarsh Kumar, M M Padhi, N Srikanth, K S Dhiman, K Santanu Tripathi
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Abstract

Background objectives: A 2.5-year placebo controlled double blind trial was conducted to investigate the safety and efficacy of AYUSH- SL, a poly- herbal Ayurvedic formulation on filarial lymphedema in different endemic areas of India. Lymphatic filariasis (LF) is caused by parasitic nematodes from Wuchereria bancrofti, Brugia malayi, or B. timori that are transmitted through mosquitoes. In Ayurveda, LF has been elaborately narrated under the heading Shlipada, and the literature also includes detailed therapeutic measures.

Methods: The multicenter, prospective, parallel group interventional study of a total of 180 participants were recruited within the duration through competitive enrollment. Diagnosed cases of grade I and grade II filarial lymphedema of Grade I and Grade II (lower extremities) were included in the trial. The study group was treated with MDA and AYUSH-SL or its placebo tablet.

Results: The control group had received MDA and a matching placebo. The primary outcome measure was the reduction in edema calculated for analysis by percentage reduction from baseline at the 4th, 12th and 24th week. Secondary outcome measures included improved quality of life (QoL), which was assessed using the Lymphatic Filariasis Specific QoL Questionnaire, and prevention of recurrence of acute episodes, which was evaluated by investigating the presence and severity of episodes in the past 4 weeks. The water displacement method for the evaluation of the efficacy of the intervention was shown to be highly significant compared to the baseline value (right leg; 3071.60 ± 970.482, 2828.40±829.339, p<0.001and Left leg; 3158.69 ± 1136.391, 2890.73 ±1077.475, p<0.001).

Interpretation conclusion: There was significant improvement of Quality of Life in the LF QoL Questionnaire (p <0.001) at each follow-up visit in both groups. Safety estimations on hematologic and biochemical parameters were within limits and or changes were not significant. The results revealed that AYUSH- SL is safe and effective for FL due to its comprehensive anti-inflammatory, antimicrobial, and anti-allergic activities.

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AYUSH-SL在接受大量药物治疗的慢性炎性淋巴水肿患者中的临床评价,一项双盲、安慰剂对照、多中心研究。
背景目的:进行了一项为期2.5年的安慰剂对照双盲试验,以调查AYUSH- SL(一种多草药阿育吠陀配方)在印度不同流行地区治疗丝虫病淋巴水肿的安全性和有效性。淋巴丝虫病(LF)是由班氏乌切里氏菌、马来布鲁氏菌或提莫里氏杆菌的寄生线虫引起的,它们通过蚊子传播。在阿育吠陀,LF已经在Shlipada的标题下进行了详细的叙述,文献还包括详细的治疗措施。方法:采用竞争入组的方法,采用多中心、前瞻性、平行组介入研究,共180人。诊断为I级和II级(下肢)丝虫性淋巴水肿的I级和II级病例纳入试验。研究组给予丙二醛和AYUSH-SL或其安慰剂片治疗。结果:对照组给予丙二醛治疗和相应的安慰剂。主要结局指标是在第4周、第12周和第24周从基线计算的水肿减少百分比。次要结局指标包括改善的生活质量(QoL),使用淋巴丝虫病特异性生活质量问卷进行评估,以及预防急性发作复发,通过调查过去4周内发作的存在和严重程度来评估。与基线值(右腿;3071.60±970.482,2828.40±829.339,p < 0.05
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来源期刊
Journal of Vector Borne Diseases
Journal of Vector Borne Diseases INFECTIOUS DISEASES-PARASITOLOGY
CiteScore
0.90
自引率
0.00%
发文量
89
审稿时长
>12 weeks
期刊介绍: National Institute of Malaria Research on behalf of Indian Council of Medical Research (ICMR) publishes the Journal of Vector Borne Diseases. This Journal was earlier published as the Indian Journal of Malariology, a peer reviewed and open access biomedical journal in the field of vector borne diseases. The Journal publishes review articles, original research articles, short research communications, case reports of prime importance, letters to the editor in the field of vector borne diseases and their control.
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