Individualized Homeopathic Medicines in Chronic Rhinosinusitis: Randomized, Double-Blind, Placebo-Controlled Trial

被引:3
|
作者
Misra, Pankhuri [1 ]
Nayak, Chintamani [1 ]
Chattopadhyay, Abhijit [1 ]
Palit, Tarun Kumar [2 ]
Gupta, Bharti [3 ]
Sadhukhan, Satarupa [4 ]
Bhar, Koushik [1 ]
Rai, Shruti [4 ]
Parewa, Maneet [5 ]
Ali, Sk Swaif [6 ]
Basu, Anamika [6 ]
Nath, Arunava [4 ]
Koley, Munmun
Saha, Subhranil
机构
[1] Govt India, Dept Mat Med, Natl Inst Homoeopathy, Minist AYUSH, Block GE,Sect 3, Kolkata 700106, W Bengal, India
[2] Govt India, Dept ENT, Natl Inst Homoeopathy, Minist AYUSH, Kolkata, W Bengal, India
[3] Govt India, Dept Paediat, Natl Inst Homoeopathy, Minist AYUSH, Kolkata, W Bengal, India
[4] Govt India, Dept Organon Med & Homoeopath Philosophy, Natl Inst Homoeopathy, Minist AYUSH, Kolkata, W Bengal, India
[5] Govt India, Dept Repertory, Natl Inst Homoeopathy, Minist AYUSH, Kolkata, W Bengal, India
[6] Govt West Bengal, Mahesh Bhattacharyya Homoeopath Med Coll & Hosp, Howrah, W Bengal, India
关键词
efficacy; homeopathy; chronic rhinosinusitis; sino-nasal outcome test; randomized controlled trial; ACUTE MAXILLARY SINUSITIS; EFFICACY; COMPLEMENTARY; THERAPY;
D O I
10.1055/s-0040-1715842
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background Chronic rhinosinusitis (CRS) is a common disorder, with up to an estimated 134 million Indian sufferers, and having significant impact on quality of life (QOL) and health costs. Despite the evidence favoring homeopathy in CRS being inadequate, it is highly popular. This trial attempts to study the efficacy of individualized homeopathy (IH) medicines in comparison with placebo in patients with CRS. Methods A double-blind, randomized (1:1), placebo-controlled, preliminary trial (n = 62) was conducted at the National Institute of Homoeopathy, West Bengal, India. Primary outcome measure was the sino-nasal outcome test-20 (SNOT-20) questionnaire; secondary outcomes were the EQ-5D-5L questionnaire and EQ-5D-5L visual analog scale scores, and five numeric rating scales (0-10) assessing intensity of sneezing, rhinorrhea, post-nasal drip, facial pain/pressure, and disturbance in sense of smell, all measured at baseline and after the 2nd and 4th months of intervention. Group differences and effect sizes (Cohen'sd) were calculated on the intention-to-treat sample. Results Groups were comparable at baseline. Attrition rate was 6.5% (IH: 1, Placebo: 3). Although improvements in both primary and secondary outcome measures were higher in the IH group than placebo, with small to medium effect sizes, the group differences were statistically non-significant (allp > 0.05, unpairedt-tests).Calcarea carbonica,Lycopodium clavatum,Sulphur,Natrum muriaticumandPulsatilla nigricanswere the most frequently prescribed medicines. No harmful or unintended effects, homeopathic aggravations or any serious adverse events were reported from either group. Conclusion There was a small but non-significant direction of effect favoring homeopathy, which ultimately renders the trial as inconclusive. Rigorous trials and independent replications are recommended to arrive at a confirmatory conclusion. [Trial registration: CTRI/2018/03/012557; UTN: U1111-1210-7201].
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页码:13 / 26
页数:14
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