Clinical Trials Logo

Irritable Bowel Syndrome clinical trials

View clinical trials related to Irritable Bowel Syndrome.

Filter by:

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.

NCT ID: NCT01553591 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.

NCT ID: NCT01551225 Completed - Clinical trials for Irritable Bowel Syndrome

Escitalopram Trial for Irritable Bowel Syndrome (IBS) Patients With Panic Disorder

Start date: January 2012
Phase: Phase 4
Study type: Interventional

This study will be executed according to a randomized double-blind placebo-controlled trial with two parallel groups, treated over the period of 6 months with escitalopram or placebo. Hypotheses: Escitalopram is more effective than placebo in the control of gastrointestinal symptoms, in irritable bowel syndrome (IBS) patients with panic disorder. Escitalopram is more effective than placebo in the control of psychiatric symptoms, in IBS patients with panic disorder.

NCT ID: NCT01545037 Completed - Clinical trials for Irritable Bowel Syndrome

Effect of BIO-K+ on Symptoms of Irritable Bowel Syndrome

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of Bio-K+ on symptoms of IBS.

NCT ID: NCT01543178 Completed - Clinical trials for Irritable Bowel Syndrome With Diarrhea

Irritable Bowel Syndrome With Diarrhea (IBS-D) Rifaximin Re-Treatment Study

TARGET3
Start date: February 2012
Phase: Phase 3
Study type: Interventional

This study will evaluate the effectiveness and safety of repeat treatment with rifaximin 550 mg three times a day in patients with IBS with diarrhea who respond to initial treatment of rifaximin 550 mg three times a day.

NCT ID: NCT01534507 Completed - Clinical trials for Irritable Bowel Syndrome

Small and Large Bowel Transit Tests Using MRI (Study 1)

Start date: November 2011
Phase: N/A
Study type: Observational

Irritable bowel syndrome, (IBS) is a common functional disorder of the gut that can be quite disabling to patients. The most common symptoms of IBS are abdominal pain or discomfort along with erratic changes in bowel habit of diarrhoea, constipation or a mixture of the two (referred to as IBS subtypes). Despite much research efforts to further understand the pathophysiology of IBS; as yet no specific biomarkers/definitive measurements have been identified that can be use to aid the diagnosis and reduce the need for unnecessary, unpleasant and expensive tests. Evidence shows that anxiety plays a part in IBS and can speed up transit time in the small bowel. In this study, the investigators hypothesise that since anxiety is a common feature of IBS, then fast small bowel transit is likely to be found in all subtypes of IBS and the difference in stool frequency and consistency in IBS subgroups are therefore likely to reflect differences in colonic function. The investigator wish to test this by measuring both small and large bowel transit times using Magnetic Resonance Imaging (MRI) and validate the results of the MRI with two methods currently used in clinical practice -The previously validated lactose-C13 Ureide breath test (for small bowel transit) and the standard radio-opaque pellet method to assess the whole gut transit (WGT) time.

NCT ID: NCT01529567 Completed - Clinical trials for Irritable Bowel Syndrome

Cognitive Behavioral Therapy With Our Without Exposure Therapy for Irritable Bowel Syndrome

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

Patients with a diagnosis of irritable bowel syndrome (IBS) are recruited by self-referral. They are randomized to two 10 weeks of internet-delivered cognitive behavioral programs. Both programs include mindfulness training, education about how excessive avoidant and control behaviors maintain IBS symptoms, and changing of these behaviors to live a richer life. One of the programs also includes instructions on how to perform systematic exposure. The hypothesis of the study is while both groups will show improvement in terms of IBS symptom severity and quality of life, the addition of systematic exposure will lead to more improvement in symptoms.