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Nosocomial Infections clinical trials

View clinical trials related to Nosocomial Infections.

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NCT ID: NCT00791583 Completed - Clinical trials for Nosocomial Infections

ED Residents MBP During CVC Placement: Sim Lab Based Training

EM CVC MBP
Start date: May 2008
Phase: N/A
Study type: Observational

1. Baseline performance in maximal barrier precaution technique of Emergency Medicine (EM) residents, certified in CVC placement, is poor 2. Simulation-based training in maximal barrier precaution technique during central venous catheter (CVC) placement will improve baseline performance of EM residents

NCT ID: NCT00787345 Completed - Clinical trials for Nosocomial Infections

Simulation-based Training for Surgery Residents in Aseptic Techniques

CVC
Start date: May 2008
Phase: Phase 3
Study type: Interventional

Central line associated bloodstream infection (CL-ABI) is an important and preventable cause of nosocomial infections and is responsible for considerable morbidity and mortality The Centers for Disease Control have published guidelines for the prevention of CL-ABI that represent a collaborative effort by a multidisciplinary coalition of professional organizations that provide evidence based recommendations to prevent catheter related infections [5]. The interventions emphasize five distinct practices, including: education and training of healthcare providers who place and care for catheters, utilizing maximum sterile barrier precautions during catheter placement.

NCT ID: NCT00617006 Completed - Clinical trials for Nosocomial Infections

Potential Nosocomial Infection Prevention Via Modification of Anesthesia Intraoperative Aseptic Practice

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

We hypothesized that by improving hand hygiene compliance in the operative environment, we would reduce horizontal transmission of pathogenic bacteria to surgical patients.

NCT ID: NCT00549393 Completed - Clinical trials for Nosocomial Infections

Study of Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit

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

The investigators propose to conduct a large clinical study to determine if daily bathing with chlorhexidine impregnated cloths will reduce the incidence of healthcare-associated infections in the Pediatric Intensive Care Unit (PICU).

NCT ID: NCT00151606 Completed - Clinical trials for Nosocomial Infections

Comparison of Two Protocols to Prevent the Acquisition of Methicillin-Resistant Staphylococcus Aureus.

Start date: December 2002
Phase: N/A
Study type: Interventional

Nosocomial infections is a major problem in intensive care units due to both growing incidence and pathogens implicated which become increasingly resistant to antibiotics. According to the Center for Disease Control (USA), Staphylococcus aureus is responsible for approximately 10% of cases. In Europe, 79% of the S.aureus strains are resistant to methicillin, a routinely used antibiotic. Recommendations for the prevention of transmission of these resistant bacteria are rarely based on controlled trials. Therefore the aim of our study is to evaluate two protocols to prevent the acquisition of methicillin-resistant S. Aureus in intensive care units: either a reinforced isolation precautions protocol or a standard precautions protocol.

NCT ID: NCT00122057 Completed - Clinical trials for Respiratory Tract Diseases

Impact of Antibiotic Treatment on Outcome in Patients With Ventilator-Associated Tracheobronchitis

Start date: June 2005
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether antibiotic treatment could reduce mechanical ventilation duration in patients with nosocomial tracheobronchitis acquired under mechanical ventilation.

NCT ID: NCT00113191 Completed - Sepsis Clinical Trials

Safety and Efficacy of Veronate® Versus Placebo in Preventing Nosocomial Staphylococcal Sepsis in Premature Infants

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

The purpose of this study is to show whether Veronate, a donor-selected staphylococcal human immune globulin intravenous (IGIV), can prevent an infection in the blood caused by staphylococcal bacteria in premature babies weighing between 500 and 1250 grams at birth. Babies are enrolled between Day of Life 3 and 5. Babies are randomized to either Veronate or placebo (50-50 chance of either). Babies can receive up to 4 doses of the study drug on Study Days 1, 3, 8 and 15 and are followed until Study Day 70 or discharge from the hospital.