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NCT ID: NCT00455806 Recruiting - Clinical trials for Helicobacter Pylori Infection

Esomeprazole, Moxifloxacin and Amoxicilin for Rescue Therapy of Helicobacter Pylori Infection

ESAMOX
Start date: January 2007
Phase: Phase 3
Study type: Interventional

Successful H. pylori eradication therapy remains a challenge in medical practice. Despite promising data for first-line, second-line and rescue treatment options based on clinical trials as well as guidelines and expert recommendations, success rates can often not be reproduced in general practice. Rescue options for patients with failed initial or second-line therapy are definitely needed. The new fluoroquinolone moxifloxacin may represent an effective and save treatment option (in combination with a PPI and amoxicillin) for rescue therapy of H- pylori positive patients.However, optimal duration of therapy (7-day course vs 14-day course) has to be determined

NCT ID: NCT00455364 Terminated - Infection Clinical Trials

Voriconazole as Prophylactic Therapy in Lung Transplant Recipients

VORI
Start date: April 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the safety and efficacy of Voriconazole with Itraconazole following lung transplantation.

NCT ID: NCT00454272 Completed - Infection Clinical Trials

Comparison of Teicoplanin and Vancomycin in Initial Empirical Antibiotic Regimen for Febrile Neutropenic Patients

Start date: January 2005
Phase: Phase 4
Study type: Interventional

The aim of the study is to evaluate the efficacy and safety of Teicoplanin versus Vancomycin as part of the initial antibiotic regimen in the therapy of patients with fever and neutropenia .

NCT ID: NCT00451386 Completed - Clinical trials for Urinary Tract Infections

Ertapenem Study in Pediatric Patients Who Have Urinary Tract Infections, Skin Infections or Community-acquired Pneumonia (0826-036)

Start date: January 2002
Phase: Phase 2
Study type: Interventional

This study will investigate the safety and efficacy of ertapenem versus ceftriaxone in pediatric patients with urinary tract infections, skin infections, or community-acquired pneumonia.

NCT ID: NCT00450632 Completed - Clinical trials for Meningococcal Infections

Creation of a Biotheque of Patients of Seine-Maritime With Meningococcal Infection

Start date: September 2005
Phase: N/A
Study type: Observational

The main objective of this study is to constitute a biotheque of patients with meningococcal disease to enable results to be interpreted and genetic factors to be determined

NCT ID: NCT00450580 Completed - HIV-1 Infection Clinical Trials

HIV-1 Infection Study of Once a Day Versus Twice a Day Protease Inhibitor in Antiretroviral Treatment Naive Adults

Start date: March 2007
Phase: Phase 3
Study type: Interventional

This is a Phase IIIB, 48 Week, multicentre, randomized, open-label, parallel group study comparing the safety and efficacy of fosamprenavir plus ritonavir 1400mg/100mg once-daily to fosamprenavir plus ritonavir 700mg/100mg twice-daily, both administered with abacavir/lamivudine 600mg/300mg once-daily in antiretroviral-naive HIV-1 infected adults. This study utilizes a group-sequential design with two stages: 1) an interim 24 week cohort analysis of approximately 200 subjects and 2) if study continuation criteria are met at this interim analysis, further enrolment of an additional 528 subjects, followed over a minimum of 48 weeks. The objectives of the study are to demonstrate 1) non-inferior antiviral activity of fosamprenavir/ritonavir 1400mg/100mg QD compared to fosamprenavir/ritonavir 700mg/100mg BID and 2) a superior fasting non-HDL lipid profile in subjects receiving fosamprenavir/ritonavir 1400mg/100mg QD.

NCT ID: NCT00448981 Completed - Clinical trials for Respiratory Tract Infections

Stopping Upper Respiratory Infections and Flu in the Family: The Stuffy Trial

STUFFY
Start date: November 2006
Phase: N/A
Study type: Interventional

Colds and flu cause much loss of work and school. The purpose of this study is to try to reduce the transmission of colds and flu among household members with one of three interventions: some educational material, educational material and use of alcohol hand sanitizers, and educational material and use of alcohol hand sanitizers as well as face masks when somebody has symptoms of the flu. We will recruit 450 households in Northern Manhattan and each household will be randomly assigned to one of these three groups. We will then follow these households for 15 months to see how often they get cold and flu symptoms. We will also look at antibiotic use practices for symptoms of colds and influenza Íž household member knowledge of prevention and treatment strategies for pandemic influenza and viral URIsÍž and rates of influenza vaccination among household members. When someone in the study has serious flu symptoms such as a high fever and cough or sore throat, we will also obtain a nasal culture (by swabbing the nose) to see if there is flu virus present.

NCT ID: NCT00448942 Completed - MRSA Colonization Clinical Trials

The Impact of Chlorhexidine-Based Bathing on Nosocomial Infections

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

The purpose of this study was to determine if the use of daily chlorhexidine bathing would decrease the incidence of MRSA and VRE colonization and healthcare associated Bloodstream Infections (BSI) among Intensive Care Unit (ICU) patients.

NCT ID: NCT00448669 Completed - HIV Infections Clinical Trials

Botswana TDF/FTC Oral HIV Prophylaxis Trial

TDF2
Start date: March 2007
Phase: Phase 2/Phase 3
Study type: Interventional

This study tested whether taking a pill of tenofovir and emtricitabine (two antiretroviral medicines) was safe for sexually-active young adults in Botswana without HIV infection and whether it reduced their risk of getting an HIV infection.

NCT ID: NCT00448604 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Viral Infections in Chronic Obstructive Pulmonary Disease (COPD) Exacerbations

VICE
Start date: May 2007
Phase: N/A
Study type: Observational

The objectives of the study are - to determine the prevalence of respiratory virus infections in COPD patients, during and outside acute exacerbation - to explore the impact of these viral infections on the outcome of these patients - to explore the association between blood procalcitonin levels and viral infections in this population.