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Community-Acquired Pneumonia clinical trials

View clinical trials related to Community-Acquired Pneumonia.

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NCT ID: NCT02018081 Completed - Clinical trials for Community-acquired Pneumonia

Pharmacokinetics of Levofloxacin in Intensive Care Unit

LEVO-PHARM
Start date: March 2012
Phase: Phase 4
Study type: Interventional

The aim of this study is 1. to describe levofloxacin pharmacokinetics in ICU patients suffering from pneumonia with taking into account physio-pathological parameters. 2. to verify clinical and bacteriological efficiency and to know if the peak/Minimum Inhibitory Concentration (MIC) ratio > 5 and Area Under Curve (AUC) /Minimum Inhibitory Concentration(MIC) ratio > 125. No therapeutic drug monitoring will be performed in this study.

NCT ID: NCT01964495 Completed - Clinical trials for Community Acquired Pneumonia

Reduction of Antibiotic Therapy by Biomakers in Patients With CAP Episodes (REDUCE Study)

REDUCE
Start date: December 5, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate two different treatment strategies in patients admitted to hospital with Community Acquired Pneumonia. The investigators hypothesize treatment according to both procalcitonin (PCT) and C-reactive protein (CRP) will be effective in reducing the length of antibiotic treatment.

NCT ID: NCT01963442 Recruiting - Clinical trials for Community Acquired Pneumonia

Short Duration Treatment of Non-severe Community Acquired Pneumonia

PTC
Start date: November 2013
Phase: Phase 2
Study type: Interventional

To investigate the non inferiority of a short lasting antibiotic treatment (3 days) when compared to a long lasting antibiotic treatment (8 days), at Day 15 after the beginning of treatment in terms of clinical efficacy, in adults admitted to emergency services for a non severe Community Acquired Pneumonia (PAC), who responded well to 3 days of beta-lactamin treatment (3GC or A/AC).

NCT ID: NCT01963000 Completed - Pneumonia Clinical Trials

Standardized Emergency Care for Community Acquired Pneumonia (CAP)

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

Community acquired pneumonia (CAP) is associated with a high in-hospital mortality. Standardization of diagnostics and adherence to sepsis bundles in the emergency department (ED) are associated with reduced mortality in patients with sepsis. Investigators examined whether the introduction of standardized care bundles and check lists in the ED are associated with a reduced mortality rate in patients hospitalized for CAP. This is an observational trial. The investigators retrospectively analyzed performance indicators of 2819 consecutive patients with CAP admitted to the Nuremberg Hospital, Germany, from 2008 to 2009. At the turn of the year, implementation of CAP care bundles took place including interprofessional education, checklists and institutionalized feedback. Primary endpoint was in-hospital mortality of CAP patients. After the implementation of CAP care bundles in the ED, mortality of affected patients was significantly lower in 2009 compared to 2008. This study should demonstrate that the implementation of a standardized CAP care bundle in the ED is associated with a risk reduction in affected patients. Standardization of diagnostic and therapeutic processes in the ED therefore improves the outcome of patients hospitalized for CAP.

NCT ID: NCT01937832 Not yet recruiting - Clinical trials for Community Acquired Pneumonia

A Phase III Study of Faropenem in the Treatment of Adult Community-acquired Bacterial Pneumonia

Start date: October 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and Efficacy of Faropenem in community-acquired pneumonia (CAP) subjects

NCT ID: NCT01886053 Completed - Clinical trials for Community Acquired Pneumonia

A Phase II Study of Faropenem in the Treatment of Adult Community-acquired Bacterial Pneumonia

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and Efficacy of Faropenem in community-acquired pneumonia (CAP) subjects,and explore its therapeutic dose.

NCT ID: NCT01883869 Completed - Pneumonia Clinical Trials

Targeting Platelet-Leukocyte Aggregates in Pneumonia With Ticagrelor

XANTHIPPE
Start date: June 2013
Phase: Phase 1
Study type: Interventional

The hypothesis to be tested is that ticagrelor (Brilinta™) will reduce platelet activation and markers of inflammation in patients with pneumonia.

NCT ID: NCT01875731 Completed - Clinical trials for Community Acquired Pneumonia

Bacterial Pneumonia Score (BPS) Guided Antibiotic Use in Children With Pneumonia and Pneumococcal Vaccine

Start date: July 2013
Phase: N/A
Study type: Interventional

The aim of this study is to test if BPS (Bacterial Pneumonia Score) guided antibiotic use in children with non severe community acquired pneumonia (CAP) and pneumoccocal vaccine will reduce antibiotic use as compared to standard care practice (current guidelines for CAP).

NCT ID: NCT01787838 Completed - Clinical trials for Community Acquired Pneumonia

Improving Pneumococcal Vaccination Rates in an Ambulatory Pre-surgical Testing Setting

Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this quality improvement project is to improve the immunization rates of an at-risk adult population seen in an ambulatory healthcare environment, through the use of targeted health education messages regarding pneumococcal immunization. Patients seen in an out-patient pre-surgical testing center will receive 1) a one-page written information sheet that outlines the benefits of pneumococcal immunization and 2) verbal reinforcement of this message, provided by the clinical staff, during the patient's interview. At-risk adult patients (as defined by Centers for Disease Control) seen in an ambulatory healthcare environment (a pre-surgical testing center) will receive a one page, "gain-framed" message that emphasizes the benefits of pneumococcal vaccinations. This educational material will be reviewed and reinforced by clinical staff during the assessment phase of the clinical visit. Among this group, there will be increased vaccination rate compared with at-risk adult patients who did not receive this communication (prospective vs retrospective data).

NCT ID: NCT01773863 Recruiting - Clinical trials for Community-acquired Pneumonia

MACCE in Hospitalized Patients With Community-acquired Pneumonia

Start date: October 2011
Phase:
Study type: Observational

Community-acquired pneumonia is the most common infection leading to hospitalization in intensive care units and the most common cause of death associated with infection disease. Epidemiological studies have shown that respiratory tract infections are associated with an increased risk for the development of acute cardiovascular and cerebrovascular events. This link is further supported by studies indicating that influenza vaccination is associated with a reduced risk of hospitalization for pneumonia as well as heart disease and cerebrovascular disease. Data connecting acute respiratory tract infections and cardiovascular events stem almost exclusively from cross-sectional or retrospective studies. Thus the real incidence and the prognostic impact of AMI, as well as the pathophysiological relationship between pneumonia and cardiovascular damage is still elusive. Inflammation plays a major role in the pathogenesis of coronary artery disease. The increased concentrations of proinflammatory cytokines together with the activation of coagulation, the down-regulation of anticoagulant mechanisms and the enhanced platelet aggregation may trigger atheroma's instability, plaque rupture and thrombus formation. Inflammation and coagulopathy are also considered universal host responses to infection in patients with severe sepsis. Thus far limited data are available on the changes in these high regulated systems, together with platelet activity in patients with CAP and their potential relationship with cardiovascular risk. This project will consist in a prospective multicenter study to investigate the incidence of major adverse cardiac and cerebrovascular events (MACCE) in hospitalized patients with CAP, its prognostic relevance and the potential relationship between enhanced cardiovascular risk and the activation of inflammation, coagulation and platelet aggregation in this setting.