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Bacterial Infections clinical trials

View clinical trials related to Bacterial Infections.

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NCT ID: NCT02361866 Completed - Clinical trials for Bacterial Infections

To Evaluate the Effectiveness(Immunogeneicity) and Safety of 'GC1107' Administered Intramuscularly in Healthy Adults

Start date: May 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness(immunogeneicity) and safety of 'GC1107' administered intramuscularly in healthy Adults.

NCT ID: NCT02339155 Completed - Clinical trials for Infections, Bacterial

Effect of Raxibacumab on Immunogenicity of Anthrax Vaccine Adsorbed

Start date: February 24, 2015
Phase: Phase 4
Study type: Interventional

This study, as a post-marketing commitment to the Food and Drug Administration, is designed to detect the effect of raxibacumab on anthrax vaccine adsorbed (AVA) immunogenicity in a healthy volunteer population. This is a randomized, open-label, parallel group, two arm study to compare the immunogenicity of AVA at 4 weeks after the first AVA dose, when AVA is administered alone or concomitantly with raxibacumab. The study is planned to enroll approximately 30 to 534 subjects in up to 3 cohorts. The total duration of the study will be approximately 26 weeks. The dates reflect cohort 1.

NCT ID: NCT02311816 Completed - Bacterial Infection Clinical Trials

Increase in Procalcitonin Kinetics May be a Good Indicator of Starting Empirical Antibiotic Treatment in Critically Ill Patients

Start date: October 2012
Phase: N/A
Study type: Observational

The value of procalcitonin change from the day before to the day when infection was suspected in predicting bacterial infection in intensive care patients.

NCT ID: NCT02311452 Completed - Pneumonia Clinical Trials

Comparative Effectiveness of Intravenous v. Oral Antibiotic Therapy for Serious Bacterial Infections

PIVVOT
Start date: January 2009
Phase: N/A
Study type: Observational

Some children get serious bacterial infections that require hospitalization and then a long course of antibiotics to completely treat the infection. Examples of these serious infections include ruptured appendicitis (when the appendix gets inflamed and bursts, releasing bacteria into the abdomen), complicated pneumonia (when an infected pocket of pus forms either in the lung or between the lung and chest wall), and osteomyelitis (an infection of the bone). To extend the duration of antibiotic therapy after discharge from the hospital, doctors will often insert a long catheter called a PICC line in the child's vein, which can stay in the body for several weeks. However, PICC lines require a fair amount of maintenance and training of caregivers in their use, require children to restrict their activities, and can lead to serious complications, such as blood stream infections and clots. An alternative to PICC lines is extending the duration of antibiotic therapy with oral antibiotics (pills or syrup) that achieve high levels of medicine in the blood and do not have the extra work, inconvenience and risks of PICC lines. Unfortunately, there are very few high quality studies that have demonstrated that oral antibiotics are just as good as intravenous antibiotics delivered via a PICC line, and so many doctors still recommend the PICC line treatment option. Also, no studies have been done to compare the impact of these two treatment options on the quality of life of the child and their caregivers. In this proposal the investigator outline a series of projects to compare oral antibiotics vs. intravenous antibiotics delivered via a PICC line in children who require prolonged (at least 1 week) home antibiotic therapy after hospitalization for three different serious bacterial infections: ruptured appendicitis, complicated pneumonia, and osteomyelitis. To see whether oral antibiotics are just as good as PICC lines, the investigators will use data collected from over 15,000 children with one of these three infections who were hospitalized at one of 43 US children's hospitals during the years 2009-2011, and determine whether PICC lines resulted in fewer rehospitalizations for treatment failure than oral therapy.

NCT ID: NCT02306330 Completed - Clinical trials for Bacterial Infections

MALDITOF Versus Routine Clinical Microbiology for Identifying Pathogens; a Randomized Diagnostic Trial

MALDITOF
Start date: December 2014
Phase: N/A
Study type: Interventional

MALDI-TOF MS is capable of directly identifying bacteria and fungi in positive blood cultures, which may be beneficial to patient management. Therefore, MALDI-TOF MS is an important new technology that is becoming routine in developed countries. It is currently unknown whether MALDITOF MS improves diagnostics, costs and patient outcomes in developing countries. This study will assess the clinical impact of a MALDITOF MS system (Maldi Biotyper, Bruker, Germany) in the resource constrained setting of Vietnam and at what cost.

NCT ID: NCT02294695 Completed - Clinical trials for Bacterial Infections

Early Procalcitonin Kinetics During Empirical Antibiotic Therapy in Critically Ill Patients

Start date: October 2012
Phase: N/A
Study type: Observational

To investigate the value of procalcitonin (PCT) kinetics between 0-8-16-24 hours after starting empirical antibiotic therapy in critically ill patients, to predict appropriate or inappropriate antibiotic treatment.

NCT ID: NCT02294175 Completed - Bacterial Infection Clinical Trials

Larval Debridement Therapy Versus Sharp Debridement to Remove Biofilm

Start date: January 2015
Phase: N/A
Study type: Interventional

This is a prospective study of Veterans with chronic lower extremity or diabetic foot ulcers who will be randomized to either a Larval Debridement Therapy group (Biobags every 4 days x 2 applications) or a Sharp Debridement Therapy group (standard or control weekly x 2) during an 8 day study period.

NCT ID: NCT02292498 Completed - Clinical trials for Pneumonia, Bacterial

Thermal Imaging to Diagnose and Monitor Suspected Bacterial Infections

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

The purpose of this study is to test the feasibility of using thermal images to diagnose bacterial pneumonia instead of a chest x-ray in the future. More specifically, the objectives of this study are: 1) to determine if thermal imaging, using a commercial thermal camera can detect areas of heat emitted from the chest in similar locations to where a chest X-ray shows focal consolidation consistent with bacterial pneumonia; 2) to evaluate whether changes in heat emitted from the chest changes over time if it is possible to obtain serial images of the chest.

NCT ID: NCT02285075 Completed - Clinical trials for Gram-Negative Bacterial Infections

Temocillin Pharmacokinetic in Hemodialysis

Start date: June 2011
Phase: Phase 4
Study type: Interventional

The current study aimed to explore the pharmacokinetics of temocillin in patients treated with haemodialysis and to demonstrated whether or not the pharmacodynamics target of a time above a MIC of 16 mg/L of more than 40 and 60 % of the dosing interval could be obtained with a dosing schedule of 1 gram/24 hours, 2 gram/48 hours and 3 gram/72 hours, all of these doses given after haemodialysis sessions only.

NCT ID: NCT02269319 Completed - Clinical trials for Bacterial Infections

MRX-I Versus Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infection

ABSSSI
Start date: February 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether MRX-I is as safe and effective as Linezolid in the treatment of adult patients with acute bacterial skin and skin structure infections