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临床试验/NCT01072916
NCT01072916已完成不适用

The Role of Serine-Proteases in Gastrointestinal Function and Irritable Bowel Syndrome

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
fecal serine protease activity

研究概览

简要总结

The proposed pilot project for this seed grant focuses on the role of intestinal serine-proteases in the pathogenesis of diarrhea-predominant IBS (D-IBS). In this study we will further assess serine-protease activity in patients with D-IBS and also explore a possible mechanism by which these proteases can lead to alterations in intestinal physiology and symptoms in these patients.

The general hypotheses for the proposed research are that (A) the levels of fecal serine-protease in patients with D-IBS are abnormally increased (B) this abnormal serine-protease activity leads to/is associated with an abnormal increase in intestinal permeability and therefore enables (C) chronic stimulation and activation of the mucosal immune system in these patients. In addition, it is aim to determine whither periodontal inflammation is associated with intestinal permeability and serine protease activity.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any sex, race, or ethnicity.
  • At least 18 years of age (no upper age limit).
  • D-IBS patients must meet Rome III criteria for IBS and must have been evaluated by a physician to exclude other diseases that could explain the symptoms. For the latter, patients self statement is acceptable (no official document is required).
  • Participation in Dr. Whitehead's 'heterogeneity of IBS' and/or Dr. Ringel's 'intestinal inflammation in patients with D-IBS' research study.

排除标准

  • Healthy controls must have no significant or recurring gastrointestinal symptoms.
  • Patients and healthy controls should not have a serious, unstable medical condition.
  • Patients and healthy controls must have had no gastrointestinal tract surgery other than appendectomy or cholecystectomy.
  • Patients and healthy controls must not be pregnant (by self-report). Pregnant women will not be allowed to participate as pregnancy can affect gastrointestinal symptoms.
  • Patients and healthy controls must not have a history of inflammatory bowel disease, celiac disease, or other diagnosis that could explain chronic or recurring bowel symptoms in IBS patients or controls.
  • Patients and healthy controls should have no history of lactose malabsorption (by self-report).
  • Patients and healthy controls should have no history of clinical symptoms of acute infections during the last 8 weeks prior to enrolment in the study.
  • Patients and healthy controls should have no history of anti-inflammatory agents including aspirin, non-aspirin, non-steroid anti-inflammatory (NSAID) or steroids in the last four weeks prior to study enrollment.
  • Patients should not intentionally consume probiotics or undergo antibiotic treatment during the last 4 weeks prior to enrolment in the study. If the subject consumed any of these medications, a washout period of 4 weeks will be required).
  • Patients must have no history of fainting or light headedness during periods of fasting.
  • Patients must not have diabetes mellitus, or any similar conditions, that would cause an adverse reaction to the sugar drink.

结局指标

主要结局

fecal serine protease activity

时间窗: protease activity determined at at recruitment

we will use an elisa-based method to measure the activity of serine proteases in fecal samples from IBS and HC subjects

次要结局

  • intestinal permeability(6hrs following recruitment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ian Carroll, PhD

Assistant Professor of Medicine

University of North Carolina, Chapel Hill

研究点 (1)

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