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临床试验/NCT02565654
NCT02565654Unknown不适用

Efficacy of Rifaximin for Diarrhea-predominant Irritable Bowel Syndrome With Positive Lactulose Hydrogen Breath Test

First Affiliated Hospital, Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2015年10月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
120
试验地点
1
主要终点
the proportion of patients who had adequate relief of global IBS symptoms

研究概览

简要总结

Irritable bowel syndrome (IBS) is a common disease and the pathogenesis of this disease includes central and peripheral mechanisms. In recent years, there were many studies suggesting that microbiota in the intestine may play an important role in the IBS.What's more, small intestinal bacterial overgrowth (SIBO) may be an important pathogenic factor for IBS and the use of antibiotics may be beneficial. Therefore, the investigators intend to explore the efficacy of rifaximin for IBS-D in Chinese population.

详细描述

Recent evidence suggests that a shift in the host-gut microbial relationship as seen in small intestinal bacterial overgrowth (SIBO) may contribute to the pathogenesis of IBS.Overgrowth of microbiota in the small intestine can cause excessive gas production and malabsorption with a variety of nonspecific symptoms, such as diarrhea, gas bloating, abdominal pain and constipation.Glucose (GBT) and lactulose (LBT) breath test have been proposed as simple, inexpensive and non-invasive diagnostic tools for detecting SIBO with respect to the gold standard (the culture of intestinal aspirates). Many antibiotics have been proposed in the last years for SIBO eradication.Rifaximin is a rifamycin derivative with antibacterial activity caused by inhibition of bacterial synthesis of RNA and which is effective against both gram-positive and -negative bacteria, including aerobes and anaerobes.As <0.1% of its oral dose is absorbed, rifaximin administration is associated to a very low side-effect incidence. However,there are still no effective and reliable treatment for IBS,so we intend to explore the prevalence of SIBO in IBS-D patients and evaluate the efficacy of rifaximin for IBS-D in Chinese population.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • aged 18-65 yr;
  • IBS-D fulfiling the ROME III criteria;
  • had undergone a colonoscopic examination within the previous 2 years;
  • had received a diagnosis of and had current symptoms of IBS, in particular, symptoms of abdominal pain and discomfort; and did not have adequate relief of global IBS symptoms and of IBS-related bloating at both the time of screening and the time of randomization.

排除标准

  • age <18 years;
  • use of antimicrobial agents within the previous 3 months;
  • known hypersensitivity to agents belonging to rifamycin and/or tetracycline families;
  • pregnancy or breast-feeding;
  • evidence of major concomitant diseases (including tumours and hepatic and ⁄ or renal insufficiency);
  • not on antibiotic treatment or probiotics for at least 4 weeks prior to undergoing the LHBT;
  • fibre supplements or laxatives 1-week prior to the LHBT test date
  • presence of endoscopic or histological alterations, which might be indicative of other disorders (e.g. celiac disease, inflammatory bowel disease, diverticulosis or diverticulitis) and contribute to IBS symptom generation,
  • evidence of major concomitant diseases (including tumours and hepatic and/or renal insufficiency)
  • unstable thyroid disease
  • bowel obstruction
  • known lactose intolerance
  • any evidence of advanced organic or psychiatric disease that may impact on the patient's compliance or adherence to the study protocol.
  • use of medications known to cause constipation (eg, narcotics, antidiarrheals, alosetron)
  • history of abdominal surgery involving the gastrointestinal tract such as appendicectomy, cholecystectomy
  • Inability to sign or rejection to informed consent

结局指标

主要结局

the proportion of patients who had adequate relief of global IBS symptoms

时间窗: 12 weeks

次要结局

  • the proportion of patients who with positive lactulose hydrogen breath test change to be negative(2 weeks)
  • the composition of patients's fecal microbiota(2 weeks)

研究者

发起方
First Affiliated Hospital, Sun Yat-Sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

XiaojunZhuang

doctor

First Affiliated Hospital, Sun Yat-Sen University

研究点 (1)

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