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Gastritis clinical trials

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NCT ID: NCT01813812 Recruiting - Chronic Gastritis Clinical Trials

A Study to Evaluate the Efficacy and Safety of DA-6034 and to Demonstrate the Non-inferiority of DA-6034

Start date: October 2010
Phase: Phase 3
Study type: Interventional

This is a multicenter, double-blinded, double-dummy, active-controlled, randomized, Phase III clinical trial to evaluate the efficacy and safety of DA-6034 and to demonstrate the non-inferiority of DA-6034 compared with Rebamipide in patients with acute or chronic gastritis. Subjects will receive 45mg, 90mg of DA-6034 and 300mg of Rebamipide, two tablets, three times a day for two weeks.

NCT ID: NCT01456273 Recruiting - Clinical trials for Functional Dyspepsia

From the Biomedical to the Biopsychosocial Model, From Theory to Practice

Start date: March 2009
Phase: N/A
Study type: Interventional

This study aims to evaluate, in patients with functional dyspepsia, a model example of medical care based upon the biopsychosocial model (called: the therapeutic encounter) compared with standard medical care based upon the biomedical model (called: medical consultation).

NCT ID: NCT01240096 Recruiting - Clinical trials for Functional Dyspepsia

Mirtazapine Versus Placebo in Functional Dyspepsia

Start date: September 2006
Phase: Phase 4
Study type: Interventional

Double-blind randomized controlled trials of 8 weeks mirtazapine 15 mg daily or placebo, followed by 8 weeks of open-label mirtazapine 15 mg daily

NCT ID: NCT01232114 Recruiting - Clinical trials for Functional Dyspepsia(FD) Was Studied

Safety Study of a Chinese Herbal Formula Simotang Oral Liquid for the Treatment of Functional Dyspepsia

SMT
Start date: October 2010
Phase: N/A
Study type: Observational

Functional dyspepsia (FD) is a common functional gastrointestinal disorder and is steadily becoming a public health problem.Simotang is a classical formula that has been used to treat gastrointestinal disorders for hundreds of years [9] and was approved as an oral liquid drug by the Chinese National Food and Drug Administration in the 1980s.In this study,patients with functional dyspepsia were divided according to the inclusive criteria into treatment group and control group randomly, who were given Simo decoction or Domperidone tablets for 14 days。And then the gastric emptying, Symptoms in plasma were observed before and after treatment in mult-center.

NCT ID: NCT01226134 Recruiting - Clinical trials for Functional Dyspepsia

Effect Of Itopride On Gastric Emptying And Accommodation In Patients With Functional Dyspepsia

EIGEAPFD
Start date: February 2009
Phase: N/A
Study type: Interventional

Pathogenesis of functional dyspepsia is poorly understood. Gastrointestinal motor abnormalities, Helicobacter pylori infection, impaired gastric accommodation to a meal, hypersensitivity of the afferent nerves of the gut, psychological disturbances and central nervous system dysfunction have been proposed. Pharmacological treatments for patients with functional dyspepsia remain unsatisfactory. Only small benefits relative to placebo have been found with histamine H2 receptor antagonists, proton pump inhibitor and Helicobacter pylori eradication. Itopride is a dopamine antagonist with acetylcholinesterase inhibitory actions. This agent is currently indicated for patients with various upper GI symptoms. This study is aimed to evaluate the effect of Itopride on gastric emptying(by 13-C Octanoic acid breath Test), accommodation (by Gastric Scintigraphy SPECT and slow nutrient drinking test)and symptoms in FD patients

NCT ID: NCT01021475 Recruiting - Clinical trials for Functional Dyspepsia

Does Visceral Manipulation Works in Treating Functional Dyspepsia?

Start date: November 2009
Phase: Phase 1
Study type: Interventional

The goal of this study is to determine if Visceral Manipulation (VM) is effective in treating Functional Dyspepsia in addition to drug therapy. Null hypothesis is that VM does not influence FD symptoms.

NCT ID: NCT01006642 Recruiting - Clinical trials for Functional Dyspepsia

Mucosal Barrier Defects in Functional Dyspepsia by Confocal Laser Endomicroscopy

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

There has been recent interest into the potential role of mucosal barrier defects in the pathophysiology of functional gastrointestinal disorders (FGIDs). There has been evidence of increased intestinal permeability in patients of IBS,and abnormal tissue resistance in NERD. Although the mucosa of Functional dyspepsia (FD) patients is endoscopically and histologically "normal," it contains ultrastructural changes, activated immune cells, along with evidence of an increased release of mediators leading to gastric dysfunction. There is now consistent evidence indicating that mucosal barrier defects allow the passage of an increased load of bacteria, antigens and toxins which, in turn evoke activation of mucosal immune responses involved in the FD symptom.

NCT ID: NCT00487955 Recruiting - Gastritis Clinical Trials

The Metabolic Contribution of the Human Microbiota to Resting Energy Expenditure

A-P-REE
Start date: June 2007
Phase: N/A
Study type: Observational

The purpose of our study is to evaluate the metabolic contribution of the human microbiota to resting energy expenditure

NCT ID: NCT00455754 Recruiting - Clinical trials for Lymphocytic Gastritis

Esomeprazole Treatment for Patients With Lymphocytic Gastritis

LYNEX
Start date: February 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether treatment with esomeprazole alone is able to heal patients with lymphocytic gastritis

NCT ID: NCT00441831 Recruiting - Clinical trials for Helicobacter Pylori Infection

The Revolutions of Helicobacter Pylori Infection, Bacterial Density, and Histological Features After Antrectomy

Start date: February 2007
Phase: N/A
Study type: Observational

Helicobacter pylori (HP) is a gram-negative bacillus responsible for one of the most common infections found in humans worldwide. By the early-to-mid 1990s, further evidence emerged supporting the link between the chronic gastritis of HP infection and malignancy in adults, specifically gastric lymphoma and adenocarcinoma. The potential of HP eradication for the prevention of gastric cancer was underlined. At the national consensus meeting held in Brussels in 1998, HP eradication was strongly recommended in past or current peptic ulcer diseases, regardless of activity, complication and post endoscopic resection of early cancer. Some patients received gastric surgery due to the complications of peptic ulcer such as bleeding or perforation in the pre-HP eradication era. Their HP infection status was not surveyed and unknown at the time. Afterward, some of them were not suggested to receive an eradication therapy and recovered from the operative procedure. According to the consensus to treat HP for a purpose to reduce the risk of gastric cancer, these patients were still under risk. There have been only a few surveys on the prevalence of persistent HP infection in patients who have undergone surgery. The aim of the study was to evaluate the prevalence and histological features of HP infection after a time course of partial distal gastric surgery.