Clinical Trials Logo

Colonic Diseases, Functional clinical trials

View clinical trials related to Colonic Diseases, Functional.

Filter by:
  • Completed  
  • Page 1 ·  Next »

NCT ID: NCT05340400 Completed - Clinical trials for Irritable Bowel Syndrome

The Prevalence and Risk Factors of Irritable Bowel Syndrome Among Adults

Start date: April 25, 2022
Phase:
Study type: Observational

This is a multicenter cross-sectional study on the prevalence of Irritable Bowel Syndrome and the risk factors associated with it. The Rome IV criteria is used for diagnosing IBS. A questionnaire-guided interview will be applied to all subjects.

NCT ID: NCT03922815 Completed - Clinical trials for Colonic Diseases, Functional

Adequacy of Anaesthesia for Colonoscopic Procedures

AoAColon
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

The aim of this randomized prospective trial is to assess the utility of Adequacy of Anaesthesia technique (Response Entropy and Surgical Pleth Index) for monitoring pain perception intraoperatively and its influence on postoperative pain perception, both patients' and operators' satisfaction in patients undergoing colonoscopic procedures under intravenous sedation using propofol and fentanyl.

NCT ID: NCT02716285 Completed - Clinical trials for Irritable Bowel Syndrome

Peppermint Oil for the Treatment of Irritable Bowel Syndrome: Optimizing Therapeutic Strategies Using Targeted Delivery

PERSUADE
Start date: August 17, 2016
Phase: Phase 3
Study type: Interventional

Peppermint oil has shown to be effective in the treatment of Irritable Bowel Syndrome (IBS) symptoms in several meta-analyses. However, the level of evidence is moderate and peppermint oil remains relatively under-used in IBS. Therefore, the investigators will conduct a multicenter randomized, placebo controlled trial to investigate the effects of an eight-week peppermint oil treatment in IBS patients according to current European Medicines Agency (EMA) / US Food and Drug Administration (FDA) guidelines. To improve efficacy and to reduce side effects, the investigators aim to study the use of a new peppermint oil formulation, a colon-targeted-delivery capsule that will release the oil in the (ileo-) colonic region specifically.

NCT ID: NCT02551029 Completed - Clinical trials for Irritable Bowel Syndrome

fMRI and Visceral Perception Upon Capsaicin Infusion

Start date: February 2016
Phase: N/A
Study type: Interventional

Brain imaging has shown abnormal brain activations in response to visceral stimulation in patients with the Irritable Bowel Syndrome (IBS) and Functional Dyspepsia (FD). To investigate the possible role of the Nucleus of the Solitary Tract (NTS), the primary relay station in the brainstem for vagal afferents, its activation in IBS and functional dyspepsia patients will be evaluated. Prior to this, an exploratory study in healthy volunteers will be conducted. This will be the first high magnetic field fMRI study (7T) evaluating the possible role of NTS activation in visceral abdominal pain. Moreover, this will be the first pharmacological fMRI study using duodenal capsaicin infusion as a chemical stimulus, which is more physiological than mechano-stimulation in the upper gastrointestinal tract.

NCT ID: NCT01887834 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy of a Multi-strain Probiotic in the Treatment of Irritable Bowel Syndrome

IBS
Start date: June 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The Canadian College of Naturopathic Medicine is conducting a research study on Irritable Bowel Syndrome (IBS), a common condition in North America. It is a long term, recurring gastrointestinal disorder that is estimated to affect 30% of the general population. IBS is characterized by abdominal pain and cramps, and bowel dysfunction such as diarrhea and bloating. The medicines that are currently used to help people with IBS are not as effective as we would like them to be. These medicines are usually only prescribed to reduce the pain of IBS and not actually treat the disorder itself. Recently, scientists have found that probiotics (beneficial bacteria that live inside humans) may help reduce the painful symptoms and diarrhea that are part of IBS. This research is being conducted to determine whether this particular combination of three probiotic bacteria (named Lactobacillus gasseri, Bifidobacterium bifidum and Bifidobacterium longum) will reduce the symptoms of severe IBS.

NCT ID: NCT01176227 Completed - Clinical trials for Irritable Bowel Syndrome

Efficacy of a Multi-strain Probiotic in the Treatment of Irritable Bowel Syndrome (IBS)

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The Canadian College of Naturopathic Medicine is conducting a research study on Irritable Bowel Syndrome (IBS), a common condition in North America. It is a long term, recurring gastrointestinal disorder that is estimated to affect 30% of the general population. IBS is characterized by abdominal pain and cramps, and bowel dysfunction such as diarrhea and bloating. The medicines that are currently used to help people with IBS are not as effective as we would like them to be. These medicines are usually only prescribed to reduce the pain of IBS and not actually treat the disorder itself. Recently, scientists have found that probiotics (beneficial bacteria that live inside humans) may help reduce the painful symptoms and diarrhea that are part of IBS. This research is being conducted to determine whether this particular combination of three probiotic bacteria (named Lactobacillus gasseri, Bifidobacterium bifidum and Bifidobacterium longum) will reduce the symptoms of IBS.

NCT ID: NCT01072903 Completed - Inflammation Clinical Trials

The Role of Intestinal Inflammation in Irritable Bowel Syndrome (IBS)

K23
Start date: January 2009
Phase: N/A
Study type: Observational

The research project addresses the following hypotheses (A) the normal balance of beneficial and detrimental commensal intestinal bacteria is deranged in IBS, with selective alterations in clinically defined patient subsets i.e., diarrhea predominant IBS (D-IBS) and post-infectious IBS (PI-IBS); (B) these changes in intestinal microflora are associated with sub-clinical mucosal inflammation and activation of the mucosal immune system; and (C) activation of the mucosal immune system leads to alterations in gastrointestinal (GI) functions (i.e., motility and sensation) and functional symptoms.

NCT ID: NCT00518349 Completed - Carcinoma Clinical Trials

Colonoscope Passive Bending Function

Start date: August 2003
Phase: N/A
Study type: Interventional

A prototype colonoscope with an extra passively bending distal section has been developed by Olympus Japan (ref. publications). The present study (2006-2007) is testing refinements of this function.

NCT ID: NCT00213317 Completed - Fecal Incontinence Clinical Trials

Effect of Lumbo-sacral Magnetic Stimulation on Colonic Motility

Start date: April 2005
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the effect of sacral nerve magnetic stimulation on the colonic motility in healthy subjects, in incontinent and constipated patients.

NCT ID: NCT00189033 Completed - Clinical trials for Colonic Diseases, Functional

Dietary Interventions in Irritable Bowel Syndrome: Soluble, Insoluble or no Fibre?

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

The purpose of this study is to assess the role of dietary fibre in Irritable Bowel Syndrome (IBS) treatment, in particular the role of increasing the content of soluble or insoluble fibres in the daily diet. The primary objective is to compare soluble (psyllium) and insoluble (bran) to placebo, administered over 12 weeks in patients with ‘probable’ or ‘definite’ Irritable Bowel Syndrome. The primary efficacy parameter is the responder rate based on weekly assessment of adequate relief of IBS symptoms. Secondary efficacy parameters include changes in IBS related symptoms (abdominal pain, bowel habits) and quality of life.