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Bacteremia clinical trials

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NCT ID: NCT02098850 Recruiting - Clinical trials for Staphylococcus Aureus Bacteremia

Staphylococcus Aureus Bacteraemia in Adults

ISAC
Start date: January 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this evaluation is to record the management and outcome of adults with S.aureus bacteraemia (SAB) across multiple European, Asian and North American sites and to identify key quality indicators associated with improved outcome.

NCT ID: NCT02020811 Recruiting - Sepsis Clinical Trials

Safety and Efficacy of Immages System in Patients Recieving IV Therapy

IV
Start date: November 2013
Phase: N/A
Study type: Interventional

The study will evaluate the functionality of IMMAGES , an intravenous infusion device system, in patients hospitalized in Bait Balev hospital. The study will aim to determine how the IMMAGES system integrates within IV infusion therapy regime and what are the advantages and disadvantages, if any, of using this system within the prescribed setting.

NCT ID: NCT01619462 Recruiting - Sepsis Clinical Trials

Safety and Immunogenicity of 10-valent and 13-valent Pneumococcal Conjugate Vaccines in Papua New Guinean Children

PCV1103
Start date: November 2011
Phase: Phase 3
Study type: Interventional

The study aims to evaluate the safety and immunogenicity of the 10-valent and 13-valent pneumococcal conjugate vaccines when administered in an accelerated schedule in Papua New Guinean children, who experience early dense upper respiratory tract colonisation with a broad range of pneumococcal serotypes, and to compare antibody titres following a booster dose of polysaccharide vaccine at 9 months with those children who received no booster at the same age.

NCT ID: NCT01511224 Recruiting - Clinical trials for Acinetobacter Bacteraemia

A Prospective Observational Study of Patients With Drug Resistant Acinetobacter Baumannii Bacteremia

ANTI-AB
Start date: August 2010
Phase: N/A
Study type: Observational

Extensively and multi-drug resistant A. baumannii (AB) represent an emerging threat in hospitals locally and worldwide. There is lack of prospective comparative clinical data to guide optimal strategy for treating such infections. Since it remains unclear how to treat bacteremia caused by AB, the present study aims to enroll patients at multiple sites with extensively drug resistant Acinetobacter species bacteremia receiving different combination therapy to assess treatment outcomes and analyze risk factors associated with mortality.

NCT ID: NCT01414400 Recruiting - Choledocholithiasis Clinical Trials

Prospective Study to Investigate the Frequency of Possible Bacterial Entry Into the Bloodstream (Bacteremia) and Infectious Complications Associated With the Use of the Spyglass Cholangioscopy System During ERCP (Endoscopic Retrograde Cholangiopancreatography).

Start date: August 2011
Phase: N/A
Study type: Interventional

The aim of this study is to prospectively evaluate the frequency of bacteremia after ERCP/cholangioscopy using the Spyglass Direct Visualization System. In addition, the frequency of cholangitis/sepsis despite use of post procedural antibiotics will be studied.

NCT ID: NCT01265095 Recruiting - Bacteremia Clinical Trials

Establish Quantitative PCR to Measure Bacteria Load of the VRE Bacteremia

Start date: December 2010
Phase: N/A
Study type: Observational

The investigators hypothesized that quantitative PCR can be used in VRE bacteremia outcome monitoring. Vancomycin-resistant enterococci (VRE) was first found in 1988 and has become an important healthcare-associated pathogen due to rapid spread, limited options for therapy and the possibility of transferring vancomycin resistance to more virulent pathogens. VRE infections not only contribute to more hospital cost and longer length of hospital stay, but also higher attributable mortality compared to those caused by vancomycin susceptible enterococci. Two different meta-analyses have shown that vancomycin resistance is an independent predictor of death among patients with enterococcal bloodstrem infections (BSIs). Despite this, few effective antibiotics are approved by the US Food and Drug Administration for the treatment of serious VRE infections. Though several studies have conducted to find the possible mortality predictors, but none has used bacterial load as a marker. Schonheyder et al. have used semiquantitative culture, and demonstrate the relationship between high bacterial load and mortality. However, it may take more than two days before culture result available, and the sensitivity of culture is greatly affected by antimicrobial treatment. Real-time PCR has been demonstrate good performance in early detection of bacteremia, and theoretically is less affected by antimicrobial usage. However, using quantitative real-time PCR to quantify VRE in blood has not been explored, yet. The objective of this study is to establish a quantitative method to measure the amounts of VRE in blood using the VRE specific van gene. And test the hypothesis that higher VRE load in blood results in higher mortality among patients with VRE BSIs. Primers and probe of VRE Real-time PCR will be constructed first. The investigators will prospective enroll patient with VRE bacteremia. Clinical data and outcome will be monitored. Bacteria load of VRE bacteremia will be measured via established real-time PCR. The outcome and the association of bacteria load of VRE bacteremia will be analyzed.

NCT ID: NCT01171547 Recruiting - Bacteremia Clinical Trials

Daptomycin Pharmacokinetics in Continuous Veno-venous Hemodiafiltration

Start date: February 2010
Phase: Phase 2
Study type: Interventional

The purpose is to investigate daptomycin pharmacokinetics in critically ill patients with suspected or verified bacteremia with Gram-positive cocci undergoing combined continuous hemodiafiltration at a filtration rate of 35ml/kg/h and to establish a dose recommendation for continuous hemodiafiltration at a filtrate rate of 35ml/kg/h.

NCT ID: NCT00901602 Recruiting - Sepsis Clinical Trials

Lebanese Interhospital Pneumococcal Surveillance Program

LIPSP
Start date: October 2005
Phase:
Study type: Observational

Streptococcus pneumoniae (pneumococcus) is a bacterium that causes severe infections in children and adults such as meningitis, pneumonia, and blood stream infection. There are many types of these bacteria defined by the type of sugar coat that they have. These are classified as serotypes. There are common serotypes that cause severe disease and are preventable by vaccination of children. Other less common types are more difficult to prevent. The investigators aim to determine the serotypes that cause invasive pneumococcal disease in Lebanon and to study their sensitivity to different antibiotics. The investigators will collect bacterial isolates from different hospitals in Lebanon isolated from the blood or spinal fluid of patients with invasive pneumococcal disease. This information will help the investigators determine the usefulness of available pneumococcal vaccines in preventing these infections. The data will be distributed to all primary care physicians treating children in Lebanon and will be shared with the Ministry of Health.

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: 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.