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临床试验/NCT00934479
NCT00934479已完成1 期

The Intestinal Microecology in Chronic Constipation

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2010年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Mayo Clinic
入组人数
21
试验地点
1
主要终点
Identification of specific microorganisms associated with chronic constipation in comparison to healthy subjects and those with C-IBS

研究概览

简要总结

The purpose of this study is to determine whether the bacteria normally present in the bowels are different in people with constipation and to see what effect the treatment with the Food and Drug Administration (FDA) - approved drug, lubiprostone, has on these bacteria.

详细描述

Chronic constipation is a common condition with a heterogeneous pathophysiology and resulting clinical manifestations. Recent evidence in the literature and collected in our laboratory confirm that there are differences in the gut microbiota between healthy individuals and those with a variety of disorders (e.g., inflammatory bowel disease, irritable bowel syndrome and obesity) suggesting that the development of certain disorders may be determined by the composition of the gut microbiota. Existing evidence warrants further investigation of the role of the microbial ecology of the human gut in constipation and an exploration of modification of the gut microbiota as a means to treat constipation by its actions on the colonic metabolism of nutrient substrates to alter colonic transit and fluid fluxes.

The proposed research will exploit our proven capability to use high-throughput molecular genomic techniques to define the intestinal microbiome in order to help define the role of the gut microbiota in chronic constipation and will explore the potential value of altering the microbiota as a management strategy in constipation. The linkage of high-throughput genomic analyses with cause-and-effect understanding of how the gut microbiota affects bowel function may lead to a reliable means to manage the gut microbiota with the intent to prevent and/or treat constipation. The immediate goals of this project are to expand on existing information about the microbial ecology in the human intestines focusing on its relationship with constipation using molecular microbiological techniques and to assess the effects on the gut microorganisms resulting from the use of the FDA-approved medication, lubiprostone. Lubiprostone is a member of a novel therapeutic class called prostones and is an orally active, bicyclic fatty acid that selectively acts on type 2 chloride channels to stimulate chloride secretion which induces a net increase in luminal fluid secretion. Unlike antibiotic, probiotic and prebiotic agents, it has no known direct effects on the gut microbiota. It is FDA-approved for the treatment of chronic constipation in men and women and for women with constipation-predominant IBS (C-IBS). The rationale for using lubiprostone to modify the gut microbiota stems from the use of similar strategies for controlling recalcitrant small intestinal bacterial overgrowth (i.e., altering fluid fluxes in the gut lumen).

We believe that this research will greatly improve our understanding of the role that the gut microbiota play in the development of constipation and potentially lead to new strategies with which to combat this common problem.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Prior gastrointestinal surgery that altered the anatomy of the esophagus, stomach, or small/large intestine (exceptions include appendectomy and cholecystectomy)
  • Gastrointestinal, cardiovascular, endocrine, renal, or other chronic disease likely to affect gastrointestinal motility (e.g., uncontrolled diabetes mellitus)
  • Females of childbearing age who are not practicing birth control and/or are pregnant or lactating (a urine pregnancy test will be performed on female subjects prior to lubiprostone use)
  • Significant untreated psychiatric disease
  • History of hypersensitivity reaction or intolerance to lubiprostone
  • Inability to stop antibiotics, probiotics, and fiber supplements 1 month prior to stool sample collection
  • Inability to stop proton pump inhibitors, histamine 2 receptor antagonists, prokinetic agents, narcotic analgesic agents, laxatives, and anticholinergic agents 2 weeks prior to stool sample collection

研究组 & 干预措施

Constipated Subjects

Experimental

Subjects with constipation included those with chronic constipation (CC) and those with constipation predominant irritable bowel syndrome (C-IBS). They completed a baseline 1-week diary of stool and defecatory characteristics, fasting breath for hydrogen and methane and a stool sample for pyrosequencing.

Following baseline test and because of differences in the FDA-approved dosing for the 2 subtypes of chronic constipation, the CC subjects received open-label lubiprostone 24 mcg orally twice daily for 4 weeks; while the C-IBS subjects received open-label lubiprostone 8 mcg orally twice daily for 4 weeks.

Following the 4-weeks treatment with lubiprostone, they completed another stool diary, fasting breath test, and stool sample for pyrosequencing.

干预措施: Lubiprostone (Drug)

结局指标

主要结局

Identification of specific microorganisms associated with chronic constipation in comparison to healthy subjects and those with C-IBS

时间窗: 5 weeks

次要结局

  • Evaluate changes in the gut microbiota after lubiprostone treatment in the chronic constipation subjects and those with C-IBS(5 weeks)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

John K. DiBaise

MD

Mayo Clinic

研究点 (1)

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