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

机译:乳酸嗜酸杆菌与安慰剂在肠易肠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道疾病,以腹痛/不适和肠道习惯改变为特征。在肠易激综合征中使用乳酸杆菌作为益生菌是基于其有趣的作用机制和良好的安全性,但由于缺乏充分设计的临床试验,对其临床疗效知之甚少。目前的临床试验方案旨在确定嗜酸乳杆菌NCFM和LAFTI L10的混合物作为益生菌改善肠易激综合征症状(LAPIBSS)的效果。80名根据罗马III标准诊断为肠易激综合征阳性的患者被纳入一项多中心、双盲、平行分组、安慰剂对照的随机试验。患者每天服用两种含有两种乳酸杆菌菌株的胶囊(5x10(9)cfu/胶囊)或安慰剂,按1:1的比例服用8周。主要结果是获得用100 mm视觉模拟量表评估的腹痛/不适评分。第二个结果是获得用100 mm视觉模拟量表测试的腹胀、胀气和隆隆声评分、综合评分、大便频率以及用布里斯托尔大便形态量表评估的大便稠度/外观。根据腹痛主要由内脏过敏引起的假设,目前的研究方案旨在提供高质量的概念验证数据,以阐明8周后食用嗜酸乳杆菌益生菌菌株混合物对减轻腹痛的效果。伦理委员会-法国西南部生物医学研究个人保护咨询委员会(编号CPP08-014a)和法国国家药品和保健品安全局(编号B80623-40)给予伦理批准。LAPBIS的研究结果将通过同行评审的出版物和科学会议进行传播。

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