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Irritable Bowel Syndrome clinical trials

View clinical trials related to Irritable Bowel Syndrome.

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NCT ID: NCT01257477 Completed - Clinical trials for Irritable Bowel Syndrome

LOTRONEX® in Severe Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)

RELIANCE
Start date: November 2010
Phase: N/A
Study type: Observational

An observational study to evaluate LOTRONEX® in women with severe IBS-D in the current clinical practice setting.

NCT ID: NCT01253408 Completed - Clinical trials for Irritable Bowel Syndrome

Effect of Cannabinoid Agonist on Gastrointestinal and Colonic Motor Functions in Patients With Irritable Bowel Syndrome (IBS)

Start date: September 2009
Phase: Phase 2
Study type: Interventional

Irritable bowel syndrome (IBS) affects about 15% of the U.S. population. There are still no effective and safe medications approved for the treatment of abdominal pain associated with bowel symptoms in IBS. This study will investigate the effects of an approved medication, Dronabinol, on the movement of food through the stomach and colon in subjects with a history of diarrhea-predominant Irritable Bowel Syndrome (D-IBS). Dronabinol is a synthetic medication (a medication made in a laboratory) related to the active ingredient of "cannabinoid or marijuana". Dronabinol is approved by the Food and Drug Administration (FDA) for preventing nausea and vomiting in patients with cancers undergoing chemotherapy. It is also used in AIDS patients with excessive weight loss for improvement in appetite and weight gain. The hypothesis in this study is that dronabinol will slow down the movement of food through the colon, and that this effect is regulated by the genes controlling the body messengers (receptors) that respond to medicinal marijuana or synthetic medicines that work on the same messengers that are present in the gastrointestinal tract and pain nerves.

NCT ID: NCT01252550 Completed - Clinical trials for Irritable Bowel Syndrome

Effects of Activia in IBS

MOSAIC
Start date: May 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the association between gut microbiota, immunology and typical pathophysiological factors in patients with IBS (all subtypes) AND to assess the effect of Activia consumption on GI symptoms provoked by a lactulose challenge test in IBS patients.

NCT ID: NCT01248013 Completed - Clinical trials for Irritable Bowel Syndrome

Irritable Bowel Syndrome Hypnotherapy

Start date: September 2005
Phase: N/A
Study type: Interventional

The primary goal of the study was whether gut focused hypnotherapy, in a group format, was successful in reduction of symptoms in patients with irritable bowel syndrome. The secondary goal was to see if any outcome predictors could be determined.

NCT ID: NCT01225237 Completed - Clinical trials for Irritable Bowel Syndrome

A Study to Evaluate Efficacy of Ramosetron on Diarrhea-predominant Irritable Bowel Syndrome (IBS) in Male Patients

Start date: October 2010
Phase: Phase 4
Study type: Interventional

A study to verify the superiority of ramosetron hydrochloride (Irribow Tablets) to placebo for male patients with diarrhea-predominant irritable bowel syndrome (D-IBS) and to evaluate its safety.

NCT ID: NCT01205100 Completed - Clinical trials for Irritable Bowel Syndrome

Treatment of Abdominal Distension by Biofeedback - a Randomized Controlled Trial

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

Background: Abdominal bloating is a frequent and bothersome complaint in patients with functional gut disorders without satisfactory treatment to date. Recent data from our laboratory indicate that abdominal distention in these patients is produced by abdomino-phrenic dyssynergia: diaphragmatic contraction associated with abdominal wall relaxation (particularly the internal oblique). In analogy to other clinical situations (e.g. functional outlet obstruction, rumination or aerophagia) behavioral treatment by means of biofeedback might be equally effective in these patients. The investigators hypothesized that abdomino-phrenic coordination and abdominal distention can be controlled by biofeedback techniques. Aim: to prove the efficacy of behavioural treatment using biofeedback techniques for abdominal distension. Randomization: Patients will be randomized into biofeedback and placebo groups. Intervention. Biofeedback: patients will be taught to control abdominothoracic muscular activity by bio-feedback using online electromyography information. Placebo: patients will be given a pill containing placebo medication. Interventions will be delivered in 3 sessions (20 min each) over 10-day period . Measurements: Sensation of abdominal distension will be assessed by means of graphic rating scales graded from 0 (no perception) to 6 (very intense sensation). The activity of the abdomino-thoracic muscles will be recorded. Abdominal distension will be measured by a metric tape fixed to a non-stretch belt placed over the umbilicus. Outcomes: Primary outcome: Change in sensation of abdominal sensation. Secondary outcomes: a) changes in thoraco-abdominal activity of the muscular walls; activity of thoraco-abdominal muscles (intercostals, diaphragm, external oblique, internal oblique, upper rectus, lower rectus) will be measured by electromyography; b) changes in girth; abdominal girth will be measured using a nonstretch belt (48mm wide) that is placed over the umbilicus. The overlapping ends of the belt will be adjusted carefully with two elastic bands to adapt constantly to the abdominal wall.

NCT ID: NCT01204515 Completed - Clinical trials for Irritable Bowel Syndrome (IBS)

Abdominal Symptom Phenotype Study in Children

ASPPNB
Start date: June 2010
Phase: N/A
Study type: Observational

Children and adults commonly suffer from recurrent abdominal (stomach) pain. One type is called irritable bowel syndrome (IBS). IBS in adults and children is one of the most common and costly health care problems in the US. Some children have pain frequently (recurrent pain) while others rarely have pain. The investigators are conducting this study to help us answer questions about the causes and treatments, and management of IBS in children. The purpose of this study is to find out if there is more than one type of IBS in children. If there is, this will be important in deciding the best treatments. The investigators also want to learn how children with IBS differ from those who do not have recurrent abdominal (stomach) pain.

NCT ID: NCT01192672 Completed - Clinical trials for Irritable Bowel Syndrome

Use of Expressive Writing in Irritable Bowel Syndrome (IBS)

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

The purpose of this study is to test whether disease-related expressive writing is effective in the treatment of Irritable Bowel Syndrome (IBS).

NCT ID: NCT01178593 Completed - Clinical trials for Irritable Bowel Syndrome

Group Hypnosis for Irritable Bowel Syndrome

IBS
Start date: April 2008
Phase: N/A
Study type: Interventional

This randomised controlled trial (RCT) aimed at assessing the efficacy of hypnotherapy in group sessions (GHT) with a 12-months follow-up.

NCT ID: NCT01177410 Completed - Clinical trials for Irritable Bowel Syndrome With Diarrhea

Mesalamine Granules for Irritable Bowel Syndrome (IBS) With Diarrhea

Start date: July 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the daily dose of mesalamine granules that will provide adequate relief from symptoms of IBS with diarrhea.