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Helicobacter Infections clinical trials

View clinical trials related to Helicobacter Infections.

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NCT ID: NCT01742429 Completed - Clinical trials for Cure Rate of Helicobacter Pylori Infection

Levofloxacin and Bismuth-containing Therapy Versus Quadruple Therapy as Second-line Treatment of Resistant Helicobacter Pylori Infection

Start date: November 2012
Phase: Phase 4
Study type: Interventional

To test the efficacy of 14 day levofloxacin and bismuth-containing second-line therapy for resistant Helicobacter pylori infection, to compare with the classical quadruple therapy.

NCT ID: NCT01735136 Completed - Clinical trials for Helicobacter Pylori Infection

Efficacy and Safety of InSan Bamboo Salt on Improvement of Helicobacter Pylori Infection

Start date: November 21, 2012
Phase: N/A
Study type: Interventional

The investigators performed a 4-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of InSan Bamboo Salt on improvement of Helicobacter pylori infection. The investigators measured improvement of Helicobacter pylori infection parameters , including 14C-UBT(Urea breath test), and subjects' symptoms, and monitored their blood pressure.

NCT ID: NCT01730352 Completed - Clinical trials for Helicobacter Pylori Infection

Helicobacter Pylori Treatment in Immune Thrombocytopenic Purpura (ITP) Patients

Start date: October 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether eradication of Helicobacter pylori infection is effective in the improvement of platelet counts in children and adolescents with chronic ITP.

NCT ID: NCT01593592 Completed - Clinical trials for Helicobacter Pylori Infection

Lactobacillus Reuteri in Management of Helicobacter Pylori Infection in Dyspeptic Patients

Start date: June 2012
Phase: N/A
Study type: Interventional

Addition of L. reuteri to the standard triple therapy improves H. Pylori treatment outcomes.

NCT ID: NCT01573975 Completed - Clinical trials for Helicobacter Pylori Infection

Comparison Between Ten Days Sequential Treatment and Traditional Three Combined Treatment of Helicobacter Pylori

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the eradication efficacy of 10-day triple therapy with 10-day sequential therapy with tetracycline or metronidazole.

NCT ID: NCT01544517 Completed - Clinical trials for Helicobacter Pylori Infection

5 Day Concomitant Versus 10 Day Sequential Therapy for Eradication of H. Pylori Infection

Start date: January 2011
Phase: Phase 3
Study type: Interventional

A five day quadruple concomitant therapy is as effective and safe as a 10 day sequential therapy for eradication of H. pylori infection.

NCT ID: NCT01513785 Completed - Clinical trials for Functional Dyspepsia

New Dual Therapy for Primary Treatment of Helicobacter Pylori Infection:a Pilot Study

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The efficacy of traditional triple therapy has been decreased to such an unacceptable level as 70% in many areas. The study is based on the hypothesis: the most important factors which influence the effect of Helicobacter pylori (H. pylori) eradication included acid suppression intensity and sensitivity of antibiotics. So the investigators chose dual therapy because it is simple and verified to be useful. Rabeprazole, as a new proton pump inhibitor (PPI), is reported to be less susceptible to the influence of genetic polymorphisms for CYP2C19. So it has a greater and faster acid suppression effect compared to other PPIs. Amoxicillin is one of effective antibiotics to H. pylori with few side effects. The antibiotic resistance of Amoxicillin is no more than 3% in China. The purpose of our trial is to evaluate and compare the efficacy and safety of dual therapy regimens with different doses of Rabeprazole for initial treatment of H. pylori infection.

NCT ID: NCT01512875 Completed - Clinical trials for Helicobacter Pylori Infection

S1119 Peruvian H. Pylori Water Contamination Study

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

The objective of this study is to elucidate the role of drinking water derived from the public source in Lima, Peru and transmission of H. pylori infection using genotypic techniques.

NCT ID: NCT01505127 Completed - H. Pylori Infection Clinical Trials

Efficacy of TAK-438, Amoxicillin and Clarithromycin in the First Line Eradication of H. Pylori

Start date: January 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to confirm the efficacy of triple therapy with TAK-438, Amoxicillin and Clarithromycin, twice daily (BID) by demonstrating its non-inferiority to triple therapy with Lansoprazole, Amoxicillin and Clarithromycin in H. pylori-positive patients with scarred gastric or duodenal ulcers.

NCT ID: NCT01456728 Completed - Clinical trials for Helicobacter Pylori Infection

Lactobacillus Reuteri ProGastria in Helicobacter Pylori-infected Adult Subjects on Proton Pump Inhibitors

Start date: January 2011
Phase: Phase 3
Study type: Interventional

The purpose of the study is to confirm that simultaneous use of L. reuteri ProGastria and omeprazole for 28 days can eradicate H. pylori in humans in the absence of antibiotics.