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Bacteremia clinical trials

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NCT ID: NCT00735813 Completed - Neoplasms Clinical Trials

Taurolidine Lock Solution in the Prevention of Catheter Related Bacteremia

Start date: April 2008
Phase: Phase 3
Study type: Interventional

Children with cancer need a long term tunnelled central venous catheter (TCVC) for the entire duration of their treatment. TCVCs are locked with heparin when not in use. The most frequent complications of long term TCVC are catheter related blood steam infections. Taurolock is a new lock that is claimed to prevent the formation of luminal biofilm in TCVCs and has been demonstrated to eradicate infected CVCs. In this study the investigators will compare TCVCs locked with heparin with TCVCs locked with Taurolock. Hypothesis: Taurolock will diminish the number of CRBSI in children with cancer compared with children with heparin lock of their CVC.

NCT ID: NCT00714402 Completed - Clinical trials for Bacterial Infections

Procalcitonin Level and Kinetics in Children With Bacterial Infections

Start date: August 2008
Phase: N/A
Study type: Observational

The purposes of this study are: 1. To determine whether procalcitonin level at admission of pediatric patients with bacterial infections can be used as a marker for prediction of defervescence and hospitalization length 2. To examine the kinetics of procalcitonin in pediatric patients with bacterial infections and persistent fever

NCT ID: NCT00695903 Terminated - Clinical trials for Infective Endocarditis

Phase 2 Study of Safety, Efficacy, and Pharmacokinetics of Higher Doses of Daptomycin and Vancomycin in MRSA Bacteremia

HDSAB
Start date: September 17, 2008
Phase: Phase 2
Study type: Interventional

The overall goals of this study are to compare the safety and efficacy of daptomycin monotherapy 10 mg/kg/day and vancomycin monotherapy dosed to achieve vancomycin trough levels of 15 to 20 μg/mL for the treatment of methicillin-resistant S. aureus bacteremia (MRSA), including right-sided infective endocarditis (RIE).

NCT ID: NCT00692848 Completed - Bacteremia Clinical Trials

Impact of Procalcitonin on the Management of Children Aged 1 to 36 Month Presenting With a Fever Without a Source

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

Serious bacterial infections are often difficult to detect in children with fever without source. Procalcitonin is a better blood marker of infection than White blood cell count and possibly than C-reactive protein. This could lead to a reduction in antibiotic prescription. Our objective is to evaluate the impact of Procalcitonin result on antibiotic prescription in children 1 to 36 month old with fever without source and our hypothesis is that it will lower the antibiotic prescription rate

NCT ID: NCT00646399 Completed - Clinical trials for Staphylococcal Sepsis

Safety and Efficacy of Pagibaximab Injection in Very Low Birth Weight Neonates for Prevention of Staphylococcal Sepsis

Start date: March 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Evaluate the safety, PK and efficacy comparing Pagibaximab Injection to placebo in preventing staphylococcal sepsis in very low birth weight infants. 1550 infants will be enrolled prior to 48 hours of life and will be randomized 1:1 to receive active drug or placebo on study days 0, 1, 2, 9, 16, and 23.

NCT ID: NCT00639197 Recruiting - Infection Clinical Trials

UGIST: Ultrasound Guided Internal Jugular Short-Term Central Venous Catheters Tunneling

UGIST
Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if tunneling standard short-term central lines for a short distance under the skin, with the assistance of ultrasound imaging, reduces the risk of central line infections for catheters placed in the neck vein. Previous work has shown that these lines can be tunneled without ultrasound guidance. We wish to determine if the use of ultrasound makes the tunneling procedure safer and easier.

NCT ID: NCT00636285 Completed - Clinical trials for Staphylococcal Sepsis

Safety and Pharmacokinetics Study in Adults for the Prevention of S. Epidermidis Infection in Low Birth Weight Infants

Start date: April 2001
Phase: Phase 1
Study type: Interventional

The purpose of this Phase 1 study is to evaluate the safety and pharmacokinetics of BSYX-A110 in a small number of healthy adult volunteers. Following the demonstration of safety in adults, this anti-Staphylococcal monoclonal antibody will then be evaluated in the target population of hospitalized low birth weight neonates.

NCT ID: NCT00631878 Completed - Clinical trials for Neonatal Staphylococcal Sepsis

Safety and Pharmacokinetics Study in VLBW Neonates With BSYX-A110

N002
Start date: November 2001
Phase: Phase 1/Phase 2
Study type: Interventional

"Phase I/II, Randomized, Double Blind, Placebo Controlled, Dose Escalating, Safety and Pharmacokinetics Study in Very Low Birth Weight Neonates of Four Doses of BSYX-A110 for the Prevention of S. epidermidis Infection." The purpose of this study is to evaluate the safety and pharmacokinetics of escalating doses of BSYX-A110 administered on Study Days 0 and 14.

NCT ID: NCT00631800 Completed - Clinical trials for Staphylococcal Sepsis

Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity Study in VLBW Neonates of BSYX-A110

N003
Start date: May 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety (including tolerability), pharmacokinetics, pharmacodynamics and clinical activity of BSYX-A110 administered in a 3-dose regimen on Study Days 0, 7, and 14.

NCT ID: NCT00622882 Recruiting - Clinical trials for Staphylococcus Aureus Bacteremia

Early Infectious Disease Consultations in Staphylococcus Aureus Bacteremia

Start date: October 2007
Phase: N/A
Study type: Interventional

The primary objective is to determine if early infectious disease (ID) consultation (defined as within 48 hours of a positive blood culture) will reduce mortality rates from Staphylococcus aureus bacteremia (SAB). This study will also determine if such consultations could reduce the duration of hospitalisation, recurrence and financial costs in patients with this infection.