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Irritable Bowel Syndrome clinical trials

View clinical trials related to Irritable Bowel Syndrome.

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NCT ID: NCT01629212 Recruiting - Clinical trials for Irritable Bowel Syndrome

Comparison of the Efficacy and Safety of Tiropramide and Octylonium in the Treatment of Irritable Bowel Syndrome

Start date: December 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study was to compare the Efficacy and Safety of Tiropramide HCl and Octylonium bromide in the Treatment of Irritable Bowel Syndrome.

NCT ID: NCT01624610 Completed - Clinical trials for Irritable Bowel Syndrome

Comparing the Effectiveness of 2 Diets for Patients With Irritable Bowel Syndrome

Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of the study is to find out if the diets often recommended for patients with Irritable Bowel Syndrome with diarrhea (IBS-D) provide adequate relief. The study will compare two diets that are used to treat IBS-D symptoms to see which one is more effective. The study will also measure the effect of these diets on the bowel flora, which are the good bacteria that inhabit the bowels in healthy people.

NCT ID: NCT01622972 Completed - Clinical trials for Functional Constipation

Mode of Action of Moviprep

Start date: September 2011
Phase: Phase 4
Study type: Interventional

The University of Nottingham have been developing new, non-invasive magnetic resonance imaging (MRI) techniques to image the bowel. Building on those studies the investigators want to study, in healthy volunteers, the effects of purging on the colon. The investigators plan two studies using their novel MRI techniques in healthy volunteers to demonstrate how doses of a preparation designed to clean the bowel alters small and large bowel water content and transit. The investigators will also define the changes induced in colonic microbiota and how these are linked to changes in transit and the structure of colonic contents. This experimental model is comparable to an episode of acute diarrhea, therefore this study will also improve their understanding of the effects of diarrhea on bowel physiology. Following from the above study, the investigators would like to extend this study on patients who have functional constipation and previously have not responded to conventional laxatives.

NCT ID: NCT01619384 Completed - Clinical trials for Irritable Bowel Syndrome

Mindfulness-Based Stress Reduction and the Microbiome

Start date: July 2010
Phase: N/A
Study type: Interventional

This proposed study aims to determine whether decreasing stress levels in persons with posttraumatic stress disorder (PTSD) can lead to a change in the intestinal microbiota, assessed 8 weeks after enrollment.

NCT ID: NCT01618292 Completed - Clinical trials for Irritable Bowel Syndrome

Cohort Study of Bowel Function Following Robotic-assisted Laparoscopic Sacrocolpopexy

Start date: January 2007
Phase: N/A
Study type: Observational

Compare changes in bowel function before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy. Compare objective anatomic outcomes before, 6 months and one year after Robotic-assisted laparoscopic sacral colpopexy.

NCT ID: NCT01613456 Completed - Clinical trials for Irritable Bowel Syndrome

Effect of Saccharomyces Cerevisiae on the Symptoms of Irritable Bowel Syndrome

Start date: December 2011
Phase: N/A
Study type: Interventional

The main purpose of this study is the effect of the probiotic yeast Saccharomyces cerevisiae CNCM I-3856 on abdominal pain or intestinal discomfort in patients presenting with the irritable bowel syndrome (IBS)

NCT ID: NCT01602575 Completed - Clinical trials for Irritable Bowel Syndrome

Neuroimaging and Biomarkers in Chronic Visceral Pain

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to use functional magnetic resonance imaging (fMRI) to evaluate brain resting state networks, responses to abdominal stimuli and the effect of MBSR Training on these measures. The goal of this study is to identify biomarkers of IBS and assess the responsiveness these biomarkers after MBSR Training. A biomarker, or biological marker, is in general a substance or measure used as an indicator of a biological state. It is a characteristic that is measured and evaluated as an indicator of normal biological processes, disease processes, or responses to a therapeutic intervention, in this case MBSR.

NCT ID: NCT01574209 Completed - Clinical trials for Irritable Bowel Syndrome

Gut Peptides and Intestinal Permeability in Celiac Disease and Irritable Bowel Syndrome

PPCD
Start date: April 2012
Phase: N/A
Study type: Observational

It is well known that the intestinal barrier is altered in celiac disease (CD), an autoimmune disease that develops in genetically predisposed subjects exposed to ingestion of wheat gliadin and of related prolamines of barley and rye. More recently, defective epithelial barrier has been implicated in the pathogenesis of other conditions such as irritable bowel syndrome (IBS). At present IBS is still considered a functional condition although low-grade inflammation has been associated with its manifestation, particularly that following infection. Different substances have been implicated in the (dis)regulation of intestinal barrier, among them zonulin seems to play a key role. Other gastrointestinal peptides are GPL-2, Ghrelin, and Epidermal growth factor (EGF). In order to shed light on the hormonal regulation of intestinal barrier function in celiac patients before undergoing a gluten free diet and possible differences with those of IBS patients, in the present study the investigators will apply the non-invasive lactulose/mannitol permeability test toward the evaluation of intestinal damage. The pattern of intestinal permeability and the GI peptides concentration will be compared in celiac patients, IBS patients and healthy controls.

NCT ID: NCT01558284 Completed - Clinical trials for Diarrhea- Irritable Bowel Syndrome

The Effect of Neu-P11 on Symptoms in Patients With D-IBS

Neu-P11
Start date: February 2012
Phase: N/A
Study type: Observational

Placebo controlled double-blind study with 40 patients who have an diarrhea-predominant IBS, 20 get Neu-P11, 20 get a placebo. Neu-P11 is a, Melatonin receptor-, Serotonin 5-HT- 1A and 5-HT- 1D - agonist and a serotonin 5-HT- 2B - antagonist.

NCT ID: NCT01553747 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy, Safety, and Tolerability of Eluxadoline in the Treatment of Participants With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-d)

Start date: May 29, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy, safety, and tolerability of different doses of eluxadoline (JNJ-27018966) compared with placebo in the treatment of participants with diarrhea-predominant irritable bowel syndrome.