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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Safety and Efficacy of Ferula asafoetida in Functional Dyspepsia: A Randomized, Double-Blinded, Placebo-Controlled Study
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Safety and Efficacy of Ferula asafoetida in Functional Dyspepsia: A Randomized, Double-Blinded, Placebo-Controlled Study

机译:阿魏菌在功能性消化不良中的安全性和有效性:一项随机,双盲,安慰剂对照的研究

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Despite the availability of various synthetic drugs for the treatment of functional dyspepsia (FD), the side effects and their cost have always created a great interest in the search for novel natural alternatives for the management of gut disorders. The present contribution reports the safety and efficacy of the kitchen spice asafoetida (Ferula asafoetida) in FD for the first time. In the double-blinded, placebo-controlled study, 43 subjects diagnosed to have moderate to severe discomforts of nonulcer FD were randomized to receive hard-shell capsules (250 mg × 2/day) of either placebo (n=22) or a food-grade formulation of asafoetida (Asafin) (n=21) for 30 days. When evaluated by a set of validated indexing tools (GSRS, GDSS, and NDI), almost 81% in the Asafin group showed significant (p < 0.01) improvement in the overall score and quality of life as compared to the placebo. At the end of the study, 66% of subjects in the Asafin group remained symptoms-free. Although the symptoms score improved significantly in both the groups (from -5.67 to -25.29 in Asafin group versus -1.55 to -6.0 in the placebo; p ≤ 0.001), the relative percentage of subjects in the Asafin group with more than 80% reduction in various symptoms were bloating (58%), appetite (69%), postprandial fullness (74%) motion sickness (75%), and digestion (77%) as compared to less than 10% nonspecific improvement in the placebo group. All the subjects remained safe with no adverse events or variations in haematological and biochemical parameters. The study was registered at http//ctri.nic.in/ (CTRI/2018/ 01/011149).
机译:尽管有各种合成药物可用于治疗功能性消化不良(FD),但其副作用及其成本一直引起人们对寻找新型天然替代品治疗肠道疾病的兴趣。本文稿首次报道了FD中的厨房调味料asafoetida(Ferula asafoetida)的安全性和有效性。在双盲,安慰剂对照研究中,被诊断患有中度至重度非溃疡性FD不适的43名受试者被随机分配接受安慰剂(n = 22)或食物的硬壳胶囊(250 mg×2 /天)等级的Asafoetida(Asafin)(n = 21),持续30天。当使用一组经过验证的索引工具(GSRS,GDSS和NDI)进行评估时,与安慰剂相比,Asafin组中将近81%的人在总体评分和生活质量上有显着改善(p <0.01)。在研究结束时,Asafin组中66%的受试者保持无症状。尽管两组的症状评分均有显着改善(Asafin组从-5.67降低到-25.29,而安慰剂组从-1.55降低到-6.0; p≤0.001),但Asafin组受试者的相对百分比降低了80%以上安慰剂组的非特异性改善少于10%,腹胀(58%),食欲(69%),餐后饱胀(74%)晕车(75%)和消化(77%)的症状有所不同。所有受试者均保持安全,没有不良事件或血液和生化指标变化。该研究已在http://ctri.nic.in/(CTRI / 2018 / 01/011149)中注册。

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