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AYUSH-SL用于接受群体服药治疗慢性炎性淋巴水肿患者的临床评估:一项双盲安慰剂对照多中心研究。

Clinical evaluation of AYUSH-SL in patients receiving mass drug administration for treatment of chronic inflammatory lymphedema: A doubleblind placebo-controlled multicentric study.

作者信息

Mitra Achintya, Bhuyan Gurucharan, Muralikrishna C, Naser S M, Ratha K K, Babu G, Venkateswarlu B, Dhoke Sujata, Bagchi Chiranjib, Singh Renu, Tripathi Arunabh, Rana Rakesh, Sharma B S, Khanduri Shruti, Gupta Bharti, Rao Bcs, Kumar Adarsh, Padhi M M, Srikanth N, Dhiman K S, Tripathi Santanu K

机构信息

Regional Ayurveda Research Institute, Ranikhet, Uttarakhand, India.

Regional Ayurveda Research Institute, Itanagar, Arunachal Pradesh, India.

出版信息

J Vector Borne Dis. 2025 Apr 1;62(2):202-210. doi: 10.4103/JVBD.JVBD_61_24. Epub 2024 Dec 5.

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 literature also includes detailed therapeutic measures.

METHODS

The multicenter, prospective, parallel group interventional study in which 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 mass drug administration and AYUSH-SL or its placebo tablet.

RESULTS

The control group had received mass drug administration and a matching placebo. The primary outcome measure was the reduction in edema calculated for analysis by percentage reduction from baseline at the 4 th , 12 th and 24 th 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 four 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 lymphatic filariasis due to its comprehensive anti-inflammatory, antimicrobial, and anti-allergic activities.

摘要

背景目的

开展了一项为期2.5年的安慰剂对照双盲试验,以研究阿育吠陀复方制剂AYUSH-SL对印度不同流行地区丝虫性淋巴水肿的安全性和有效性。淋巴丝虫病(LF)由班氏吴策线虫、马来布鲁线虫或帝汶布鲁线虫等寄生线虫引起,通过蚊子传播。在阿育吠陀医学中,LF在“Shlipada”标题下有详细记载,文献中也包括详细的治疗措施。

方法

这项多中心、前瞻性、平行组干预研究通过竞争性招募在规定时间内招募了180名参与者。确诊为I级和II级(下肢)丝虫性淋巴水肿的病例被纳入试验。研究组接受群体服药及AYUSH-SL或其安慰剂片剂治疗。

结果

对照组接受了群体服药及匹配的安慰剂。主要结局指标是计算水肿减轻情况,通过第4周、12周和24周时相对于基线的减轻百分比进行分析。次要结局指标包括生活质量(QoL)改善,使用淋巴丝虫病特异性QoL问卷进行评估,以及预防急性发作复发,通过调查过去四周内发作的存在情况和严重程度进行评估。与基线值相比,干预效果评估的排水法显示具有高度显著性(右腿;3071.60±970.482,2828.40±829.339,p<0.001;左腿;3158.69±1136.391,2890.73±1077.475,p<0.001)。

解读结论

两组在每次随访时,淋巴丝虫病QoL问卷中的生活质量均有显著改善(p<0.001)。血液学和生化参数的安全性评估在正常范围内,或变化不显著。结果显示,AYUSH-SL因其全面的抗炎、抗菌和抗过敏活性,对淋巴丝虫病安全有效。

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