The Efficacy and Safety of Herbal Unani Formulations in Chronic Plaque Psoriasis: A Single-arm Clinical Trial

被引:0
|
作者
Fatima, Gulnaz [1 ]
Husain, Nazim [2 ]
Jabeen, Arzeena [3 ]
Uddin, Qamar [3 ]
Kazmi, Munawwar Husain [4 ]
机构
[1] State Unani Med Coll, Dept Med Unani, Prayagraj, Uttar Pradesh, India
[2] Luqman Unani Med Coll Hosp & Res Ctr, Dept Med Unani, Vijayapura, Karnataka, India
[3] Natl Res Inst Unani Med Skin Disorders, Dept Med Unani, Hyderabad, India
[4] Hamdard Univ, Unani Med, Gazaria, Bangladesh
关键词
SEVERITY; LINN;
D O I
暂无
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background center dot Despite there being advanced treatment options, psoriasis remains an incurable and recurring disease. Noteworthy scholars of Unani (Greco-Arab) medicine have proposed many drugs and formulations for psoriasis but the scientific evidence on the same is scarce. Hence, trial formulations were selected for the study. Primary Study Objectives center dot This study was designed to evaluate the efficacy and safety of two herbal Unani formulations, Ma jun Mundi and Qairuti Karnab, in the management of chronic plaque psoriasis (CPP). Methods/Design center dot This open-label, single-arm clinical trial was conducted on 33 participants, of whom 30 completed the 12-week treatment course. Setting center dot This study was conducted at the Central Research Institute of Unani Medicine (CRIUM), Hyderabad, Telangana, India, from 01 August 2018 to 25 May 2019. Participants center dot Participants of any gender aged 18 to 65 years with clinically diagnosed CPP and psoriasis area severity index (PASI) >= 10% were included in the trial. Interventions center dot The participants received 5 g of Ma.jun Mundi (a semisolid preparation) orally, twice daily with water, followed by the topical application of Qairuti Karnab (a homogenous paste) to cover the lesions over 12 weeks. Outcome Measures center dot The primary outcome measure was the change in PASI determined pre- and post-trial in terms of mean and percentage reduction. Secondary outcome measures were changes in patient global assessment (PGA) on a 100 mm visual analog scale, investigator global assessment (IGA) on a 6-point scale, and subjective parameters including erythema, induration, scaling, and itchiness. Results center dot The analysis revealed a significant reduction in the PASI score, with 12 subjects (40%) achieving PASI 75 and 3 subjects (10%) achieving PASI 90. Significant improvements were also observed in secondary outcome measures with no adverse events. Conclusion center dot The findings of the study indicate that the trial formulations exhibit a notable anti-psoriatic effect without any adverse effects. The formulations are worthy of further evaluation as an alternative treatment for CPP.
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页码:210 / 215
页数:6
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