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Lactobacillus acidophilus versus placebo in the symptomatic treatment of irritable bowel syndrome: the LAPIBSS randomized trial

机译:乳酸杆菌与安慰剂在肠易激综合征的症状治疗中:Lapibss随机试验

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Irritable bowel syndrome is a chronic functional gastrointestinal disorder characterized by abdominal pain/discomfort and altered bowel habits. The use of Lactobacilli as probiotics during irritable bowel syndrome is based on their interesting mechanisms of action and their excellent safety profile but little is known about their clinical efficacy due to the lack of adequately designed clinical trials. The current clinical trial protocol aims to determine the effects of a mixture of Lactobacillus acidophilus NCFM and LAFTI L10 as probiotics to improve irritable bowel syndrome symptoms (LAPIBSS). Eighty patients with a positive diagnosis of irritable bowel syndrome according to Rome III criteria were recruited to a multicentre, double-blinded, in parallel groups, placebo-controlled randomized trial. Patients were provided with a daily dose of two capsules with two strains of Lactobacilli (5x10(9)cfu/capsule) or placebo for 8 weeks on a 1: 1 ratio. The primary outcome is to obtain scores of abdominal pain/discomfort assessed with a 100-mm visual analogue scale. The secondary outcome is to obtain scores of bloating, flatus and rumbling tested with a 100-mm visual analogue scale, composite score, stool frequency and stool consistency/appearance assessed with the Bristol Stool Form scale. According to the hypothesis that abdominal pain is mainly the result of a visceral hypersensitivity, the current study protocol aims to provide high quality proof of concept data to elucidate the efficacy of a consumption of a mixture of Lactobacillus acidophilus probiotic strains after 8 weeks, for decreasing abdominal pain. Ethical approval was given by ethics committee French Consultative Committee for the Protection of Individuals in Biomedical Research of the South West (Number CPP08-014a) and ANSM (French National Agency for Medicines and Health Products Safety-Number B80623-40). The findings from LAPBISS will be disseminated through peer-reviewed publications and at scientific conferences.
机译:肠易激综合征是一种慢性功能性胃肠疾病,其特征在于腹痛/不适和肠习惯改变。在肠易肠综合征期间使用乳杆菌作为益生菌是基于他们有趣的行动机制及其优秀的安全性,但由于缺乏适当设计的临床试验,他们的临床疗效很少。目前的临床试验方案旨在确定乳酸杆菌和LAFTI L10作为益生菌的混合物的影响,以改善肠易激综合征症状(LAPIBS)。根据罗马III标准的急性肠综合征患者急诊诊断的八十名患者被招募到多期,双盲,并行组,安慰剂控制随机试验。患者在每日剂量的两种胶囊中提供两种胶囊(5×10(9)CFU /胶囊)或安慰剂8周的乳杆菌(5×10(9)CFU /胶囊)或1周的比例。主要结果是获得以100mm视觉模拟量表评估的腹痛/不适的评分。二次结果是获得用100mm的视觉模拟刻度,复合评分,粪便频率和粪便一致性/外观获得的膨胀,舱窗和隆隆声和用布里斯托尔粪便形式等级评估的膨胀。根据腹痛的假设主要是内脏超敏的结果,目前的研究方案旨在提供高质量的概念数据证明,以阐明8周后乳酸杆菌患者益生菌菌株混合物的疗效的疗效腹痛。道德批准由道德委员会法国法国咨询委员会保护南部的生物医学研究委员会(Number CPP08-014A)和澳门州(法国国家药品和医疗保健品安全号码B80623-40)。 Lapbiss的调查结果将通过同伴审查的出版物和科学会议传播。

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