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Gastritis clinical trials

View clinical trials related to Gastritis.

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NCT ID: NCT00764374 Completed - Dyspepsia Clinical Trials

A Long-term, Open-label, Uncontrolled Trial of YM443 (Z-338) in Patients With Functional Dyspepsia

Start date: August 2008
Phase: Phase 3
Study type: Interventional

To examine the safety and efficacy of Z-338 (YM443) after long-term administration in patients with functional dyspepsia, and also to examine the pattern of long-term administration.

NCT ID: NCT00761358 Completed - Clinical trials for Functional Dyspepsia

To Verify the Efficacy of Z-338 in Subjects With Functional Dyspepsia

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to verify the superior efficacy of Z-338 to placebo in subjects with Functional Dyspepsia, focusing on the assessment of subjective symptoms.

NCT ID: NCT00663897 Completed - Clinical trials for Functional Dyspepsia

Lansoprazole Versus Mosapride for Functional Dyspepsia

Start date: May 2008
Phase: Phase 4
Study type: Interventional

Functional dyspepsia is a common symptom complex with significant impact on quality of life. There is no standard treatment for functional dyspepsia but therapeutic efficacy of proton pump inhibitor (PPI) and prokinetic agent have been proved in subsets of patients. This study has two aims: - first is to compare the therapeutic efficacy of lansoprazole (a PPI) and mosapride (a prokinetic agent) for functional dyspepsia - second is to investigate whether different subgroups of functional dyspepsia (e.g., epigastric pain syndrome and postprandial distress syndrome) respond differently to PPI and prokinetic agent.

NCT ID: NCT00613665 Completed - Lymphoma Clinical Trials

Safety and Immunogenicity of Chiron's Investigational H. Pylori Vaccine in Healthy Adults

Start date: February 2001
Phase: Phase 1
Study type: Interventional

This study was designed to investigate the safety and immunogenicity of Chiron's investigational H. pylori (HP3) vaccine

NCT ID: NCT00599677 Completed - Clinical trials for Functional Dyspepsia

Randomized Controlled Trial of Acupuncture for Functional Dyspepsia

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of the study is to testify the efficacy of treating functional dyspepsia with acupuncture, and provide evidence for the hypothesis that "Acupuncture effect is based on meridians, and gathering of meridian Qi is the key point."

NCT ID: NCT00579410 Completed - Inflammation Clinical Trials

Comparison of Acid Reflux at Two Levels in the Esophagus Using the BRAVO Capsule

Start date: May 2004
Phase: N/A
Study type: Observational

The purpose of this research is to study the level of acid exposure above the gastroesophageal junction and the distal esophagus in patients with reflux symptoms using a capsule type acid measurement system. Patients with reflux symptoms are likely to have more acid reflux just above the junction of the stomach and the esophagus that may help to improve the diagnosis of gastroesophageal reflux disease (GERD). This may help better treat the reflux symptoms.

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.

NCT ID: NCT00333372 Completed - Clinical trials for Functional Dyspepsia

To Evaluate the Efficacy of Z-338 in Subjects With Functional Dyspepsia

Start date: April 2006
Phase: Phase 2
Study type: Interventional

To Evaluate the efficacy of Z-338 in subjects with Functional Dyspepsia, focusing on the assessment of subjective symptoms in order to further determine the optimal dosage and efficacy parameters for PhaseIII clinical trials.