The Efficacy of an Oral Formulation of Glycyrrhiza glabra, Viola odorata, and Operculina turpethum as an Add-on Therapy for Mild-to-moderate Childhood Asthma: A Randomized Placebo-Controlled Clinical Trial.

IF 0.8 Q4 PHARMACOLOGY & PHARMACY
Faezeh Rabbani, Mohsen Raeisi, Majid Keivanfar, Ali Saffaei, Ali Mohammad Sabzghabaee
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引用次数: 1

Abstract

Objective: We aimed to evaluate the efficacy of an oral combined tablet of Glycyrrhiza glabra, Viola odorata, and Operculina turpethum (Anti-Asthma®) as an add-on therapy for the relief of the severity of symptoms in mild-to-moderate childhood asthma.

Methods: This randomized placebo-controlled clinical trial was performed on 60 children and adolescents with chronic mild-to-moderate childhood asthma. Patients were randomly divided into cases who received Anti-Asthma® oral combined tablets 2 tablets twice dailt for 1 month and controls, received placebo tablets identically the same to Anti-Asthma® (2 tablets, twice daily, for 1 month) as add-ons to their standard therapy according to the guideline. The severity and frequency of cough attacks and shortness of breath, respiratory test indices (based on spirometry), and the extent of disease control and treatment adherence were measured clinically by validated questionnaires at the beginning and after the study.

Findings: Respiratory test indices improved and the severity of activity restriction decreased significantly in the cases compared to the controls However, the mean difference before and after the study was significantly different between the cases and controls only for the number and severity of coughs and the severity of activity restriction. In the scores of the Asthma Control Questionnaire, the cases group had a significant improvement compared to the controls.

Conclusion: Anti-Asthma® oral formulation may be effective as an adjunct add-on treatment in the maintenance therapy of mild-to-moderate childhood asthma.

Abstract Image

甘草、堇菜和甲壳草口服制剂作为轻中度儿童哮喘附加治疗的疗效:一项随机安慰剂对照临床试验。
目的:我们旨在评估一种口服甘草、堇菜和猪皮草联合片(抗哮喘®)作为缓解轻中度儿童哮喘症状严重程度的附加治疗的疗效。方法:本随机安慰剂对照临床试验对60例慢性轻中度儿童哮喘儿童和青少年进行研究。患者随机分为两组,一组服用抗哮喘®口服联合片剂2片,每日2次,持续1个月;另一组服用与抗哮喘®相同的安慰剂片剂(2片,每日2次,持续1个月),作为标准治疗的补充。在研究开始时和研究结束后,通过有效的问卷临床测量咳嗽发作和呼吸短促的严重程度和频率、呼吸试验指标(基于肺活量测定法)、疾病控制程度和治疗依从性。结果:与对照组相比,病例呼吸试验指标改善,限制活动严重程度明显降低,但仅咳嗽次数和严重程度以及限制活动严重程度与对照组相比,研究前后的平均差异有显著差异。在哮喘控制问卷的得分上,病例组与对照组相比有显著改善。结论:抗哮喘®口服制剂可作为轻中度儿童哮喘维持治疗的辅助治疗手段。
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来源期刊
Journal of Research in Pharmacy Practice
Journal of Research in Pharmacy Practice PHARMACOLOGY & PHARMACY-
自引率
0.00%
发文量
8
审稿时长
21 weeks
期刊介绍: The main focus of the journal will be on evidence-based drug-related medical researches (with clinical pharmacists’ intervention or documentation), particularly in the Eastern Mediterranean region. However, a wide range of closely related issues will be also covered. These will include clinical studies in the field of pharmaceutical care, reporting adverse drug reactions and human medical toxicology, pharmaco-epidemiology and toxico-epidemiology (poisoning epidemiology), social aspects of pharmacy practice, pharmacy education and economic evaluations of treatment protocols (e.g. cost-effectiveness studies). Local reports of medication utilization studies at hospital or pharmacy levels will only be considered for peer-review process only if they have a new and useful message for the international pharmacy practice professionals and readers.
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