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Helicobacter Infections clinical trials

View clinical trials related to Helicobacter Infections.

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NCT ID: NCT02466919 Completed - Clinical trials for Helicobacter Pylori Infection

Study of Levofloxacin-based Concomitant Therapy for H. Pylori Eradication in Diabetic Patients

Start date: May 2014
Phase: Phase 4
Study type: Interventional

The study aims to evaluate H. pylori eradication rate in diabetic patients by using novel 10-day levofloxacin-based concomitant therapy compared with conventional 10-day sequential therapy.

NCT ID: NCT02449941 Completed - Clinical trials for Helicobacter Infections

Helicobacter Pylori and Proton Pump Inhibitor

Start date: March 2014
Phase: N/A
Study type: Observational

The purpose of this study is to know the distribution of HP in stomach before use of PPI, during use of PPI, and after stop of PPI.

NCT ID: NCT02401477 Completed - Clinical trials for Helicobacter Infections

Dual Therapy With High Doses of Ilaprazole and Amoxicillin for Helicobacter Pylori Infection

Start date: December 2014
Phase: Phase 4
Study type: Interventional

This study assessed eradication rate of dual therapy with high doses of Ilaprazole 40mg BID and Amoxicillin 750mg QID for 14 days on Helicobacter pylori infection.

NCT ID: NCT02395458 Completed - Clinical trials for Helicobacter Infections

Efficacy on Helicobacter Pylori Eradication With Two Antibiotic Regimens

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Clinical trial to compare efficacy on eradicating Helicobacter pylori with two antibiotic strategies: sequential with amoxicillin and omeprazole 5 days and clarithromycin with metronidazole and omeprazole 5 days or omeprazole with clarithromycin and amoxicillin 14 days.

NCT ID: NCT02373280 Recruiting - Clinical trials for Helicobacter Infection

The Efficacy of the 7 Days Tailored Therapy as the 1st Eradication of H. Pylori Infection

Start date: August 2014
Phase: N/A
Study type: Interventional

To compare the eradication success rate between 10-days sequential therapy and 7-days tailored therapy based on H. pylori culture and antimicrobial susceptibility testing.

NCT ID: NCT02368470 Recruiting - Clinical trials for Helicobacter Pylori Infection

Randomized Study on Efficacy of Gemifloxacin-based Regimen for Helicobacter Pylori Infection

Start date: February 2015
Phase: Phase 3
Study type: Interventional

New generations of fluoroquinolones, like levofloxacin and moxifloxacin, exhibit a broad-spectrum activity against Gram-positive and Gram-negative bacteria, and have been successfully introduced into the treatment of Helicobacter pylori infection. However, it was suggested that resistance to fluoroquinolones has been increasing in the Korean population and the resistance is most likely mediated through point mutation in gyrA. Gemifloxacin (FACTIVE®) is an enhanced-affinity, broad-spectrum fluoroquinolone suitable for once-daily, oral dosing. In vitro studies have shown that gemifloxacin displays potent activity against Gram-positive organisms, whilst retaining good activity against Gram-negative organisms. Gemifloxacin is the most potent member of the quinolone class against S. pneumoniae with activities 16-64 times greater than those of ciprofloxacin and ofloxacin and 2-8 times greater than those of moxifloxacin. Importantly, gemifloxacin displays potent in vitro activity against strains of S. pneumoniae with known resistance to β-lactams, macrolides and other members of the quinolone class. This potent activity is believed to be due to the enhanced affinity of gemifloxacin for topoisomerase IV, the major fluoroquinolone target in S. pneumoniae. Furthermore, gemifloxacin displays potent activity against H. influenzae and M. catarrhalis and atypical organisms such as L. pneumophila, C. pneumoniae and M. pneumoniae. It has proven particularly effective in respiratory and urinary tract infection.

NCT ID: NCT02359942 Completed - Clinical trials for Helicobacter Pylori Infection

The Diagnostic Validity of the Urea Breath Test

Start date: March 1, 2015
Phase: N/A
Study type: Interventional

1. To compare the diagnostic accuracy of the 13C-Urea breath test between using the citric acid as test meal and controlled group by endoscopic biopsy methods(histology, CLOtest and H. pylori culture). 2. To compare the delta value of 13CO2 results between before and after ingestion of citric acid as test meal.

NCT ID: NCT02359435 Completed - Clinical trials for Helicobacter Pylori Infection

Comparison of 12-day Reverse Hybrid Therapy and 12-day Standard Triple Therapy for Helicobacter Pylori Infection

REHYTRI
Start date: October 2012
Phase: N/A
Study type: Interventional

Reverse hybrid therapy is a one-step two-phase treatment for Helicobacter pylori infection with less cost than standard triple therapy. Whether reverse hybrid therapy can replace standard triple therapy as the recommended first-line treatment is unknown. The investigators compared the efficacy of 12-day reverse hybrid therapy and 12-day standard triple therapy in first-line treatment.

NCT ID: NCT02359331 Terminated - Clinical trials for Helicobacter Infection

The Efficacy of the 7 Days Tailored Therapy as 2nd Rescue Therapy for Eradication of H. Pylori Infection

Start date: August 2014
Phase: N/A
Study type: Interventional

As increasing the antibiotics resistance, the effectiveness of traditional Helicobacter pylori (H. pylori) therapies has been declined coincidentally. In this study, the investigators evaluated the efficacy of H. pylori eradication between a 7 days personalized therapy for H. pylori infection based on the results of antibiotics resistance by using H. pylori culture and minimal inhibitory concentration (MIC) and the 14 days bismuth contained quadruple 2nd rescue regimens, and the investigators analyzed the prevalence of the antibiotic resistance after 1st eradication of H. pylori in the tailored therapy group.

NCT ID: NCT02352701 Completed - Clinical trials for Helicobacter Infections

Efficacy and Safety of Basic Triple Therapy Including Ilaprazole on the First Line Eradication Treatment of H.Pylori

Start date: December 2012
Phase: Phase 4
Study type: Observational

This study compared efficacy and safety of basic triple therapy including Ilaprazole 10mg, Levofloxacin 500mg and Amoxicillin 1000mg BID for 10 days on the first line eradication treatment of H.pylori