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A pilot study on the effect of a symbiotic mixture in irritable bowel syndrome: An open-label, partially controlled, 6-month extension of a previously published trial

机译:一项共生混合物对肠易激综合症的影响的初步研究:一项公开发表的,部分控制的,先前发表的试验延长了6个月的研究

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Background: In recent years, the efficacy of probiotics has received considerable attention in the treatment for irritable bowel syndrome (IBS). In this regard, a symbiotic mixture (Probinul?) has shown beneficial effects. The aim of this study was to extend the previously published 4-week randomized, double-blinded, placebo-controlled study of this symbiotic mixture. Methods: This is an open-label prospective, partially controlled, 6-month extension period pilot study in which patients continued to receive the symbiotic mixture (Group 1) or were switched from placebo to symbiotic mixture (Group 2) using cyclic administration (last 2 weeks/month). The primary endpoints were the overall satisfactory relief of bloating and flatulence (assessed as proportions of responders). The secondary endpoints were evaluation of the symptom severity scores (bloating, flatulence, pain and urgency) and bowel function scores (frequency, consistency and incomplete evacuation). Results: Twenty-six IBS patients completed the 6-month extension period (13 patients in Group 1 and 13 patients in Group 2). In the per-protocol analysis, the proportions of responders across time were not significantly different in the groups but in Group 2, there was an increased percentage of responders for flatulence (p = 0.07). In addition, the score of flatulence was reduced significantly during the 6-month treatment period in Group 2 (p < 0.05), while no other significant differences were detected. Conclusions: Treatment with this symbiotic mixture was associated with persistence of relief from flatulence or new reduction in flatulence in the present 6-month long extension study. These results need to be more comprehensively assessed in large, long-term, randomized, placebo-controlled studies.
机译:背景:近年来,益生菌的功效在肠易激综合征(IBS)的治疗中受到了相当大的关注。在这方面,共生混合物(Probinul?)已显示出有益的作用。这项研究的目的是扩展以前发表的这种共生混合物的4周随机,双盲,安慰剂对照研究。方法:这是一项开放性,前瞻性,部分对照,为期6个月的扩展期前期研究,在该研究中,患者继续接受共生混合物(组1)或通过循环给药从安慰剂改为共生混合物(组2)(最后一次2周/月)。主要终点是总体令人满意的腹胀和肠胃气胀缓解(按缓解者比例评估)。次要终点是对症状严重程度评分(腹胀,肠胃气胀,疼痛和尿急)和肠功能评分(频率,稠度和不完全排空)进行评估。结果:26名IBS患者完成了6个月的延长期(第一组13例,第二组13例)。在按方案分析中,各组中随时间变化的应答者比例没有显着差异,但在第2组中,肠胃气胀的应答者百分比有所增加(p = 0.07)。此外,在第2组的6个月治疗期间,肠胃气胀评分显着降低(p <0.05),而未发现其他显着差异。结论:在目前的为期6个月的长期研究中,使用这种共生混合物治疗与持续消除肠胃气胀或肠胃气胀的新减少有关。这些结果需要在大型,长期,随机,安慰剂对照研究中进行更全面的评估。

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