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Pneumonia clinical trials

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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 (Brilintaâ„¢) will reduce platelet activation and markers of inflammation in patients with pneumonia.

NCT ID: NCT01881672 Completed - ICU Patients Clinical Trials

Syndrome and Aspiration Pneumonia in Intensive Care

SPIRE
Start date: November 2012
Phase: N/A
Study type: Observational

Inhalation is a common condition in patients with impaired their awareness requiring protection of the upper airway by endotracheal intubation. This inhalation may lead to chemical pneumonitis and/or bacterial pneumonia. Only the latter requires the administration of antibiotics. Patients developing such a bacterial pneumonia, has a mortality, duration of mechanical ventilation and length of ICU stay increased. However, the proportion of patients with such bacterial pneumonia, bacterial ecology and morbidity that are little known. The aim of this study is to determine the frequency of bacterial pneumonia in patients admitted to the ICU for coma and treated with mechanical ventilation

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: NCT01875692 Completed - Clinical trials for Pneumonia, Ventilator-Associated

Can we Better Understand the Development of VAP and Eventually Predict and Prevent it?

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

Pathogens of ventilator-associated pneumonia (VAP) come from colonizers of the trachea. The hypothesis of the investigators is that during the first days of intubation, independently of the use of antibiotics, there is a change in the oro-pharyngeal flora leading to the selection of one pathogen in the trachea, that will finally be the cause of VAP. The investigators designed a prospective study including 300 patients intubated for more than 3 days, with daily analysis of oro-pharyngeal juice and tracheal aspirate by culture and metagenomics, in order to determine if this microbiological surveillance permits: 1. To predict a high risk to develop a VAP in the next 48h and even to predict its agent 2. To better understand the development of VAP by studying the evolution of the "respiratory flora" in the context of intubation

NCT ID: NCT01868113 Completed - Bacterial Pneumonia Clinical Trials

Inhaled Corticosteroids in U-5 Children With Acute Respiratory Infection in Uganda: A Randomised Trial

ICS
Start date: December 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to find out whether adjunct treatment with inhaled corticosteroids lead to faster improvement and reduce mortality of children under 5 years of age admitted to hospital with ALRI.

NCT ID: NCT01858974 Completed - Pneumonia Clinical Trials

Fast Identification of Pathogen in the Setting of Pneumonia Using Multiplex PCR

Start date: June 2013
Phase: N/A
Study type: Observational

With this study the investigators want to determine, if a fast identification of germs, causing infections of the lower respiratory tract, is possible through the use of Multiplex PCR technology - a method that allows on time detection of bacteria in medical specimen by identifying DNA sequences that are known to be specific for the respective microbe. Therefore aspiration samples from the respiratory tracts of ventilated patients, which are suspected to develop such an infection, will be collected and analyzed by using a multiplex PCR (polymerase chain reaction) application situated on the intensive care unit. The investigators want to determine if Multiplex PCR diagnostic could be a faster alternative to conventional microbiological methods. The results of the Multiplex PCR analyses therefore will be compared with results of conventional microbiological methods.

NCT ID: NCT01839474 Completed - Pneumonia Clinical Trials

CPAP Survival Study in Ghana

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

The purpose of this study is to determine if the use of a continuous positive airway pressure (CPAP) machine (a device that blows air into the lungs) decreases the chance of a child dying from difficulty breathing.

NCT ID: NCT01826968 Completed - Pneumonia Clinical Trials

Alveolar Recruitment Maneuver During Cesarean Section Improves Lung Compliance

CSRecGHPyr
Start date: January 2013
Phase: Phase 2
Study type: Interventional

The investigators tested the hypothesis that alveolar recruitment maneuver during cesarean section and in women under general anesthesia improves lung compliance and gas exchange. The investigators applied recruitment maneuver and positive end expiratory pressure (PEEP) 8 cmH2O. The maximum alveolar pressure limit (Ppeak)was 45 cmH2O during the recruitment maneuver. The primary end point of the study is the improvement of the lung compliance measured as volume difference/pressure difference (dv/dp) or ml/cmH2O

NCT ID: NCT01819935 Completed - Pneumonia Clinical Trials

Clinical Outcomes of Methicillin Resistant Staphylococcus Aureus (MRSA) Hospital-Based Pneumonia

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

The purpose of this non-interventional, retrospective study of existing data is to evaluate clinical outcomes related to Methicillin-resistant Staphylococcus aureus hospital based pneumonia by treatment and among subpopulations.

NCT ID: NCT01818089 Completed - Pneumonia Clinical Trials

Monitoring of Lung Sounds of Patients With Pneumonia

Start date: April 2013
Phase: N/A
Study type: Observational

The aim of this study is to investigate if any correlation between lung sounds of pneumonia patients and the clinical development or therapy of the pneumonia exists.