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Helicobacter Pylori clinical trials

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NCT ID: NCT01510730 Completed - Helicobacter Pylori Clinical Trials

Helicobacter Pylori Eradication After Endoscopic Resection of Gastric Tumors

Start date: January 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Helicobacter pylori eradication could reduce the new tumor development after endoscopic resection of gastric tumor.

NCT ID: NCT01278901 Not yet recruiting - Helicobacter Pylori Clinical Trials

The Effect of PPI Therapy on the Result of Helicobacter Pylori Diagnostic Tests

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

STUDY PROTOCOL: The study will include 30 patients ages 18-80y that had a gastroscopy for various reasons. The patients should not be on PPI therapy . If during the gastroscopy there are some pathologies that require a second look endoscopy after some weeks of therapy (ulcers or esophagitis), the investigators will repeat the gastroscopy within a month. During the first gastroscopy a biopsy will be taken for histological examination and for a rapid urease test and an urea breath test will be done soon after the procedure. If one of the tests is positive the investigators postulate that the Helicobacter pylori is actually present. After the gastroscopy the patient is given a full dose of PPI (as indicated) and helicobacter tests are repeated in the next endoscopy (under PPI therapy) . Any positive test that become negative in the second endoscopy is considered false negative.

NCT ID: NCT01273441 Completed - Helicobacter Pylori Clinical Trials

Study Comparing Sequential and Concomitant Therapy for Helicobacter Pylori Eradication in Routine Clinical Practice

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

Helicobacter pylori is the main cause of chronic gastritis, peptic ulcer and gastric tumors (adenocarcinoma and lymphoma). The cure of the H. pylori infection prevents recurrence of duodenal and gastric ulcer and improves dyspepsia in a significant proportion of cases, so it is cost-effective. Eradication therapy has changed over time. The usually recommended pattern in the consensus conferences has traditionally been triple therapy, composed by the combination of 2 antibiotics (clarithromycin plus amoxicillin or metronidazole) and a proton pump inhibitor (PPI) for 7-14 days. Recent meta-analyses have that the current global eradication rate after standard triple therapy is less than 80%. Several European studies have found even lower eradication rates, with 35-40% of cases resulting in treatment failure. Treatment failure leads to a second treatment and a new diagnostic test to confirm eradication.

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: NCT00596401 Completed - Gastric Cancer Clinical Trials

The Preventive Effect of Helicobacter Pylori Eradication on the Development of Gastric Cancer

Start date: September 2007
Phase:
Study type: Observational

Recently, the preventive effect of Helicobacter pylori (Hp) eradication treatment on the incidence of gastric cancer has been reported. By Hp eradication treatment being performed for Hp-infected people in Iijima town, we will evaluate whether the incidence of gastric cancer and/or the medical care cost can be reduced as compared with those in the previous years.

NCT ID: NCT00475527 Withdrawn - Helicobacter Pylori Clinical Trials

Helicobacter Pylori and Iron Deficiency: Prevalence of Association and Effect of Therapy

Start date: n/a
Phase: Phase 4
Study type: Interventional

Iron deficiency anemia (IDA) is a major health problem in children, effecting up to 20% of young children. Helicobacter pylori (HP) infection is also reported to be prevalent in children. Several large epidemiologic studies support an association between HP infection and lower iron stores. Other small studies suggest improvement in anemia following HP treatment. We assume that the prevalence of HP infection in Israeli children diagnosed with IDA is high and that that adding therapy for HP in those children will improve the response to iron deficiency.

NCT ID: NCT00467155 Withdrawn - Helicobacter Pylori Clinical Trials

Helicobacter in The Gambia (Part 2)

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

The purpose of this study is to examine Helicobacter pylori bacteria in the stomach fluids of children who are hospitalized and receiving nutritional care via nasogastric feeding (tube from the nose to the stomach) to treat malnutrition. The H. pylori strains from Gambian children may differ genetically from the strains found in the stomachs of adults from the same community. The fluid samples will be examined for H. pylori bacterial infections that may make children sick and unable to absorb food. Ninety hospitalized Gambian children, less than 2 years of age, requiring a nasogastric feeding tube will have stomach fluid samples taken via the gastric tube. Thirty mothers of children who are positive for H. pylori bacteria will provide a sample of stomach fluid. This study may help develop treatments to heal the stomach and improve child growth. This study will be conducted at the Medical Research Council of Great Britain Research Laboratories and Clinical Facility in Fajara.

NCT ID: NCT00466700 Completed - Helicobacter Pylori Clinical Trials

Helicobacter in The Gambia (Part 1)

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

H. pylori infection causes the stomach to become inflamed. The problem usually begins in childhood and leads to stomach problems in adult life. Study participants will be residents of The Gambia, West Africa, and will be studied at the Medical Research Council of Great Britain facility in Fajara, The Gambia. Up to 75 adults 18 years and older and 20 malnourished children 6 months to 2 years of age, who are undergoing endoscopy as part of their medical care, will be studied. (Endoscopy is when a thin, lighted device is used to look inside the body.) During this study procedure, tiny pieces of tissue, called biopsies, will be taken from the stomach and checked for H. pylori infection. Participants found to be infected will be given antibiotic treatment. Participation in the study will last approximately 72 hours.

NCT ID: NCT00306280 Recruiting - Helicobacter Pylori Clinical Trials

Feasibility Study of Phototherapy System to Treat H Pylori

Start date: March 2006
Phase: N/A
Study type: Interventional

This purpose of this study is to determine whether phototherapy can be used to safely and effectively treat H pylori.

NCT ID: NCT00281047 Recruiting - Helicobacter Pylori Clinical Trials

The Influence of FP-10 on the Eradication Rates of H. Pylori by a Triple Therapy

Start date: January 2006
Phase: Phase 2/Phase 3
Study type: Interventional

FP-10 is a food ingredient derived from milk casein. FP-10 can inhibit H. pylori to attach to the gastric epithelium. FP-10 has been made clear to decrease the intragastric urease activity (which is assumed to be produced by H. pylori) measured by the urea breath test. FP-10 can also detach H. pylori from gastric epithelium. We have hypothesized that FP-10 increases the eradication rates by a triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin.