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Irritable Bowel Syndrome clinical trials

View clinical trials related to Irritable Bowel Syndrome.

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NCT ID: NCT01505777 Completed - Clinical trials for Irritable Bowel Syndrome Without Diarrhea

Exploratory Clinical Study to Evaluate the Optimal Dosage of Mosapride and Probiotics in Irritable Bowel Syndrome Without Predominant Diarrhea

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

The purpose of this study is to Evaluate the Optimal Dosage of Mosapride (Medirac) and Probitics in Irritable Bowel Syndrome Without Predominant Diarrhea.

NCT ID: NCT01497847 Completed - Clinical trials for Irritable Bowel Syndrome With Diarrhea

Post-Infectious Irritable Bowel Syndrome (PI-IBS)

PI-IBS
Start date: March 2010
Phase: N/A
Study type: Observational

Purpose: - identification of factors predisposing for Post-Infectious Irritable Bowel Syndrome (PI-IBS) development after an episode of traveler's diarrhea - identification of systemic (serum) and local (biopsy) changes in infectious and immunological activity during infection and correlation with Irritable Bowel Syndrome (IBS) symptoms, persisting after traveler's diarrhea Design: - 4 study visits: before traveling, 2 weeks after traveling, 6 months after traveling, 12 months after traveling - at each study visit following investigations: blood collection, stool collection, questionnaires, rectal biopsy

NCT ID: NCT01494233 Completed - Clinical trials for Irritable Bowel Syndrome

A Multi-Center Trial to Determine the Safety and Efficacy of LX1033 in Subjects With Diarrhea-Predominant Irritable Bowel Syndrome

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

The objective of this study is to evaluate the safety and efficacy of LX1033 over a range of dose levels in subjects with diarrhea-predominant Irritable Bowel Syndrome (IBS).

NCT ID: NCT01483287 Completed - Clinical trials for Irritable Bowel Syndrome

The Effects of Added Enzyme α-Galactosidase at a Carbohydrate-rich Meal in Irritable Bowel Syndrome (IBS)

Start date: November 2011
Phase: Phase 0
Study type: Interventional

IBS (irritable bowel syndrome) is a functional gastrointestinal disorder which is characterized by recurrent pain and/or discomfort, altered stool form, and abdominal distension. It has been established that food items such as beans, peas, lentils, peppers, and onions can increase gas production. What these have in common is that they all contain large amounts of complex carbohydrates. The enzymes in the small intestine are not able to fully digest these large molecules, which in turn are fermented by the colonic microflora. This fermentation is conducted through the production of short chain fatty acids and gases such as hydrogen and methane. Alpha-Galactosidase is an enzyme that has the ability to break down these indigestible carbohydrates to galactose and sucrose in the small intestine and to facilitate the absorption and minimize the gas production from bacteria in the colon. The aim of this study is to assess if the gastrointestinal symptoms, above all problems from gas and distension, is alleviated when the enzyme α-Galactosidase (present in Nogasin capsules) is ingested with food.

NCT ID: NCT01476995 Completed - Hypertension Clinical Trials

Prognostic Indicators as Provided by the EPIC ClearView

GBMC
Start date: September 2010
Phase: N/A
Study type: Observational

The objective of this study is to determine whether the finger tip images captured by the EPIC ClearView device, when analyzed via the ClearView software, produce a Response Scale that characterizes trends consistent with known diagnoses identified by medical doctors. Specifically, the investigators hypothesize that the organ system involving any of a series of known active diagnoses will be identified in the EPIC ClearView Response Scale report with the intention of providing potential triage capabilities.

NCT ID: NCT01475929 Terminated - Clinical trials for Irritable Bowel Syndrome

Effect of Probiotic Supplement on Bowel Function

IBS2
Start date: June 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to analyse the effect of probiotic supplement on symptoms of irritable bowel syndrome.

NCT ID: NCT01471379 Terminated - Clinical trials for Irritable Bowel Syndrome

Milnacipran (Savella) in Irritable Bowel Syndrome (IBS)

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

Purpose: The investigators are proposing to examine the use of Savella® (Milnacipran) for treating irritable bowel syndrome (IBS) in women. Participants: Eligible participants will meet the Rome III diagnostic criteria for IBS. Procedures: This study will observe patients treated with Savella® as well as patients treated with a placebo (pill with no active drug). The investigators will monitor and compare several patient and symptom related outcomes, as well as evaluate health related quality of life, psychological distress and related psychosocial measures to determine if the addition of Savella® improves clinical pain response as well as secondary outcomes including quality of life.

NCT ID: NCT01457378 Completed - Clinical trials for Irritable Bowel Syndrome

Gastrointestinal Symptoms in Healthy Subjects and Patients With Irritable Bowel Syndrome

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

The aim of this study performed in Irritable Bowel Syndrome (IBS) subjects and healthy patients is to demonstrate the ability of composite score of frequency of gastrointestinal symptoms to discriminate healthy subjects and IBS patients. The properties of this questionnaire of composite score of gastrointestinal symptoms frequency will be compared to other validated questionnaires (severity of IBS symptoms and HRQoL).

NCT ID: NCT01436760 Completed - Clinical trials for Irritable Bowel Syndrome

Genetic Contribution of Pain and Inflammation in IBS

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

The goal of the study is to identify possible polymorphisms on the loci of candidate genes that may be involved in modulation of pain and inflammation in irritable bowel syndrome.

NCT ID: NCT01418066 Completed - Clinical trials for Irritable Bowel Syndrome

Ayurvedic Herbs in Diarrhea Predominant Irritable Bowel Syndrome

AHIB
Start date: August 2011
Phase: N/A
Study type: Interventional

In the present study the investigators are trying to evaluate the effect of Murraya koenigii leaves, Punica granatum and Curcuma which is administered to the patients in a combined form as tea. This study will help to evaluate the effect of these preparations scientifically in improving the IBS symptoms.