Individualized Homeopathic Medicines in the Treatment of Tinea Corporis: Double-Blind, Randomized, Placebo-Controlled Trial

被引:2
|
作者
Laskar, Bakibillah [1 ]
Paul, Swapan [1 ]
Chattopadhyay, Abhijit [1 ]
Karuppusamy, Avaranjika [1 ]
Balamurugan, Dharshna [1 ]
Bhakta, Puja [2 ]
Das, Sourav [1 ]
Pal, Siddhartha [3 ]
Singh, Navin Kumar [4 ]
Koley, Munmun [5 ]
Saha, Subhranil [6 ]
机构
[1] Natl Inst Homoeopathy, Dept Mat Med, Block GE,Sect 3, Kolkata 700106, W Bengal, India
[2] Natl Inst Homoeopathy, Dept Homoeopathy Pharm, Kolkata, W Bengal, India
[3] Natl Inst Homoeopathy, Dept Organon Med & Homoeopath Philosophy, Kolkata, W Bengal, India
[4] West Bengal Univ Hlth Sci, Calcutta Homoeopath Med Coll & Hosp, Dept Repertory, Govt West Bengal, Kolkata, India
[5] Govt West Bengal, East Bishnupur State Homoeopath Dispensary, Dept Hlth & Family Welf, Chandi Daulatabad Block Primary Hlth Ctr, Kolkata, W Bengal, India
[6] Govt West Bengal, Dept Repertory, DNDe Homoeopath Med Coll & Hosp, Kolkata, W Bengal, India
基金
美国国家卫生研究院;
关键词
homeopathy; itching; placebo; randomized controlled trial; Skindex-29; Tinea corporis;
D O I
10.1055/s-0042-1750799
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Introduction Tinea corporis (TC; ringworm or dermatophytosis) is a superficial skin infection caused by Microsporum , Epidermophyton and Trichophyton genera of dermatophytes. We compared the effects of individualized homeopathic medicines (IHMs) in fifty-millesimal (LM) potencies against placebo in TC. Methods A double-blind, randomized, placebo-controlled, two parallel arms trial was conducted on 62 individuals suffering from TC at the National Institute of Homoeopathy, India. Participants were randomized in a 1:1 ratio to receive either IHMs in LM potencies or identical-looking placebos for a period of 3 months. The primary outcome measure was the number of participants showing complete disappearance of skin lesions after 3 months. Secondary outcomes were a numeric rating scale (NRS) measuring intensity of itching and the Skindex-29 questionnaire (overall, and three sub-scales-degree of symptoms, psychological functioning, emotional status). All were assessed at baseline and every month, up to 3 months. The intention-to-treat sample was analyzed to detect inter-group differences using two-way repeated measures analysis of variance after adjusting for baseline differences. Results The primary outcome revealed no improvement in either of the groups ( chi (2) = 0.012, p = 0.999). Inter-group differences in some of the secondary outcomes favored IHMs against placebo-itching NRS (mean group difference after 3 months: -0.7 (95% confidence interval [CI], -1.1 to -0.4; p = 0.001); Skindex-29 overall (mean group difference after 3 months: 3.2 [95% CI, -0.6 to 7.0; p = 0.009]), Skindex-29 degree of symptoms (mean group difference after 3 months: 0.9 [95% CI, -0.2 to 1.9; p = 0.007]); and Skindex-29 psychological functioning (mean group difference after 3 months: 1.7 [95% CI, 0-3.4; p = 0.002]). Conclusion Results were negative on the primary outcome; however, secondary outcomes included some statistically significant results favoring IHMs against placebo after 3 months.
引用
收藏
页码:74 / 84
页数:11
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