Urgesi R, Casale C, Pistelli R, Rapaccini G L, de Vitis I
Department of Internal Medicine and Gastroenterology, Complesso Integrato Columbus, Catholic University of the Sacred Heart, School of Medicine, Rome, Italy.
Eur Rev Med Pharmacol Sci. 2014;18(9):1344-53.
Irritable bowel syndrome (IBS) is a chronic gastrointestinal (GI) disorder that affects 15-20% of the Western population.
There are currently few therapeutic options available for the treatment of IBS. The aim of this study is to evaluate the efficacy and the safety of a medical device containing a combination of Simethicone and Bacillus coagulans in the treatment of IBS.
This is a monocentric double-blind, placebo-controlled parallel group clinical trial. Adult subjects suffering from IBS as defined by Rome III criteria were enrolled. Bloating, discomfort, abdominal pain were assessed as primary end point. Subjects received the active treatment or placebo 3 time a day after each meal for 4 weeks of study period. Subjects were submitted to visit at Day 0 (T1), at Days 14 (T2) and 29 (T3).
Fifty-two patients were included into the study. Intragroup analysis showed a significant reduction of the bloating, discomfort and pain in Colinox® group (CG) compared to placebo group (PG). Between group analysis confirmed, at T1-T3, significant differences between CG and PG in bloating and discomfort.
Simethicone is an inert antifoaming able to reduce bloating, abdominal discomfort. Literature offers increasing evidence linking alterations in the gastrointestinal microbiota and IBS and it is well known that probiotics are important to restore the native gut microbiota. The Colinox medical device is specifically targeted against most intrusive symptom of IBS (bloating) and it is also able to counteract the most accredited ethiopathogenetic factor in IBS (alterations of intestinal microbiota).
This is the first randomized double-blind placebo-controlled clinical trial demonstrating the efficacy and safety of a combination of simethicone and Bacillus coagulans in treatment of IBS.
肠易激综合征(IBS)是一种慢性胃肠道疾病,影响着15%至20%的西方人群。
目前治疗IBS的治疗选择很少。本研究的目的是评估一种含有西甲硅油和凝结芽孢杆菌组合的医疗器械治疗IBS的有效性和安全性。
这是一项单中心双盲、安慰剂对照平行组临床试验。纳入符合罗马III标准定义的IBS成年受试者。将腹胀、不适、腹痛作为主要终点进行评估。受试者在研究期间每餐饭后每天接受3次活性治疗或安慰剂,共4周。受试者在第0天(T1)、第14天(T2)和第29天(T3)接受随访。
52名患者纳入研究。组内分析显示,与安慰剂组(PG)相比,西甲硅油和凝结芽孢杆菌复方制剂组(CG)的腹胀、不适和疼痛明显减轻。组间分析证实,在T1 - T3时,CG和PG在腹胀和不适方面存在显著差异。
西甲硅油是一种惰性消泡剂,能够减轻腹胀和腹部不适。文献提供了越来越多的证据表明胃肠道微生物群的改变与IBS有关,并且众所周知益生菌对于恢复肠道原生微生物群很重要。西甲硅油和凝结芽孢杆菌复方制剂医疗器械专门针对IBS最困扰人的症状(腹胀),并且还能够对抗IBS中最公认的病因学因素(肠道微生物群改变)。
这是第一项随机双盲安慰剂对照临床试验,证明西甲硅油和凝结芽孢杆菌组合治疗IBS的有效性和安全性。