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Irritable Bowel Syndrome clinical trials

View clinical trials related to Irritable Bowel Syndrome.

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NCT ID: NCT01370720 Recruiting - Clinical trials for Irritable Bowel Syndrome

Safety and Efficacy Study of PEA and Polydatin on Intestinal Inflammation and Visceral Hyperalgesia in IBS Patients

CMD-IBS09(2)
Start date: February 2010
Phase: Phase 2
Study type: Interventional

Despite the pathophysiology of IBS remains largely unsettled, several mechanisms have been proposed to explain symptom generation. These include psychosocial factors, altered gastrointestinal motor function and altered perception of visceral stimuli because of chronic low-grade inflammation and increased nociceptive mediator release by inflammatory cells, particularly mast cells. The aim of this pilot study is to provide evidence of: 1. intestinal mast cell (MC) infiltration and activation in IBS patients; 2. down-modulation of MC activation by the oral administration of the association of palmitoylethanolamide (PEA) and polydatin in IBS patients.

NCT ID: NCT01304355 Recruiting - Clinical trials for Irritable Bowel Syndrome

An Assessment of Cognitive Function in Irritable Bowel Syndrome

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

Irritable bowel syndrome (IBS) is a common disorder affecting up to 20% of the general population. Despite the prevalence of the disorder, it remains poorly understood. This is reflected in a symptom based diagnostic scheme, the lack of a suitable biological marker and inadequate treatment options. Current knowledge suggests the disorder is as a result of a dysregulated brain-gut axis, a complex construct describing the bidirectional communication systems underpinning normal gastrointestinal functioning. The investigators hypothesize here that the disruption of this brain-gut axis is facilitated by an increased degradation of tryptophan along the kynurenine pathway. This metabolic abnormality has the potential to impact on both GI and CNS signaling through its effects on serotonergic signaling and the impact of metabolites like kynurenic acid and quinolinic acid on cognitive processes respectively. Previous data from our laboratory indicated increased tryptophan degradation in IBS patients and suggested the metabolites produced as putative biological markers of the condition. In this study the investigators aim to reconcile cognitive impairment in IBS with GI and CNS symptom severity and kynurenine pathway metabolites. The investigators will establish these baseline measures in IBS compared to control subjects. A battery of cognitive assessments will be carried out using a computerized testing system. Standardized rating scales will be used to assess GI and CNS symptom severity. GC-MS/MS, a recently acquired technology platform in our laboratory, will be used to quantify plasma quinolinic acid levels.

NCT ID: NCT01286597 Recruiting - Clinical trials for Irritable Bowel Syndrome

The Effects of Lactose Intolerance on Gastrointestinal Function and Symptoms in a Chinese Population

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

Lactose is a carbohydrate found in milk,and Lactase Deficiency (LD) is a condition in which the small intestine cannot digest this carbohydrate due to absent or insufficient amounts of lactase.Individuals with LD may be intolerant of lactose in the diet and experience abdominal cramps, bloating and diarrhea; however the response is variable.Some tolerate moderate amounts of lactose without adverse effect,whereas others experience severe symptoms in response to even small doses. These problems may be representative of wider issues regarding individual tolerance to diet containing ubiquitous poorly absorbed, fermentable carbohydrates (such as: fructose, fructans)and be relevant to symptom generated in patients with diarrhea predominant irritable bowel syndrome (D-IBS). This project will investigate the effects of diet,lifestyle stress and psychiatric dietary on the development of functional gastrointestinal symptoms. Lactose will be used to assess tolerance to dietary challenge, a test that is particularly relevant in a Chinese population with a high prevalence of lactase deficiency.

NCT ID: NCT01255345 Recruiting - Clinical trials for Irritable Bowel Syndrome

Female Chronic Pelvic Pain

Female CPP
Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the frequency and severity of chronic pelvic pain (CPP) in adult women living in Copenhagen Country and Zealand Country (total population 2,4 million), Denmark, in relation to selected factors, such as basic demographic and clinical factors, health related quality of life, physical activity and abnormal muscular findings in the pelvic area.

NCT ID: NCT01243853 Recruiting - Clinical trials for Irritable Bowel Syndrome

Alpha-galactosidase Enzyme and Irritable Bowel Syndrome

ALFA
Start date: December 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether alpha-galactosidase enzyme is affective in alleviating the symptoms of irritable bowel syndrome (IBS).

NCT ID: NCT01167673 Recruiting - Clinical trials for Irritable Bowel Syndrome

The Effect of Coltect (Selenium, Curcumin and Green Tea) on Irritable Bowel Syndrome

Start date: April 2011
Phase: Phase 2
Study type: Interventional

Irritable bowel syndrome (IBS) causes many symptoms, including abdominal pain, irregular bowel movements and bloating. It may be caused by loe degree inflammation of the intestine. The ingredients of coltect which contains green tea, selenium, and curcumin have been proven very safe and have anti inflammatory and anti oxidant activity. The aim of the study is to see whether the use of Coltect can improve symptoms in IBS patients.

NCT ID: NCT01131442 Recruiting - Clinical trials for Irritable Bowel Syndrome

Immunological Change and the Single Nucleotide Polymorphism (SNP) in Children With Irritable Bowel Syndrome (IBS)

Start date: November 2008
Phase: N/A
Study type: Observational

Currently, the pathophysiology of Irritable bowel syndrome( IBS) remains unclear . The purpose of this study is want to investigate the immunological changes in the children with IBS.

NCT ID: NCT00883077 Recruiting - Ulcerative Colitis Clinical Trials

Assessment of Colonic Permeability by Confocal Laser Endomicroscopy

Start date: April 2009
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the efficacy of confocal laser endomicroscopy in assessment of colonic permeability against conventional sugar absorption test.

NCT ID: NCT00775060 Recruiting - Clinical trials for Irritable Bowel Syndrome

Maastricht IBS Cohort

Start date: September 2009
Phase: N/A
Study type: Observational

To set up a cohort of at least 400 IBS patients in order to identify different patient subgroups according to phenotypical and genotypical patterns and To set up a biobank for future translational studies on the pathophysiology of IBS, in order to identify genetic factors to unravel the pathogenesis of IBS and to provide novel therapeutic targets.

NCT ID: NCT00742118 Recruiting - Clinical trials for Irritable Bowel Syndrome

Effects of the Soluble Mediators of Mastocytes on the Intestinal Epithelial Barrier and of the Enteric Nervous System During the Syndrome of the Irritable Bowel

Start date: February 2008
Phase: N/A
Study type: Interventional

Patients with irritable bowel syndrome (IBS) have increased intestinal permeability. In addition, mucosal soluble mediators are involved in the pathophysiology of pain in IBS. The investigators aimed to investigate: 1. paracellular permeability in colonic biopsies of IBS patient 2. the ability of soluble factors from colonic biopsies to reproduce in vitro these alterations