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Pneumonia, Ventilator-Associated clinical trials

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NCT ID: NCT00938002 Completed - Clinical trials for Ventilator Acquired Pneumonia

Study to Determine Quicker Methods of Diagnosing Pneumonia Caused by a Breathing Machine in Critically Ill Patients

Start date: July 2009
Phase:
Study type: Observational

Critically ill patients on a breathing machine are at risk of developing a type of pneumonia called Ventilator Acquired Pneumonia (VAP). The purpose of this study is to determine if regular lung rinses sent for microbiological testing can reduce the time to diagnose VAP. The study also plans to test the accuracy and speed of a new technology, using multiplexed automated digital microscopy, to identify the germs causing the VAP.

NCT ID: NCT00935285 Active, not recruiting - Clinical trials for Ventilator-Associated Pneumonia

Ventilator-Associated Pneumonia (VAP) in Intensive Care Unit (ICU)

Start date: July 2009
Phase: N/A
Study type: Observational

Ventilator-associated pneumonia (VAP) is very common in the intensive care unit (ICU), affecting 9 to 40% of ICU patients and mortality rates range from 20 to 50% and may reach more than 70% when the infection is caused by multi-resistant and invasive pathogens. The most common pathogens that cause VAP are the Gram(-) bacteria. Findings indicate that TLRs serves as an important signal in the generation of protective innate responses to bacterial pathogens of the lung and that is required for effective innate immune responses against Gram-negative bacterial pathogens. There is genetic evidence that mutations in TLRs increase the risk of developing nosocomial infections. Understanding the TLR system should offer invaluable opportunity for manipulating host immune responses.

NCT ID: NCT00934934 Terminated - Clinical trials for Ventilator Associated Pneumonia

Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment

CANTREAT
Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether the effect of treating Candida spp. isolated in the respiratory tract secretions of patients with a clinical suspicion of ventilator associated pneumonia (VAP) on clinical outcomes will be feasible and supported by biomarker data obtained.

NCT ID: NCT00893763 Completed - Clinical trials for Mechanical Ventilation Complication

Strategies To Prevent Pneumonia 2 (SToPP2)

SToPP2
Start date: September 2008
Phase: Phase 2
Study type: Interventional

Ventilator-associated pneumonia (VAP) is a serious complication in mechanically ventilated critically ill patients. The intervention tested in this project (swabbing the mouth with chlorhexidine before the endotracheal tube is inserted) could reduce the risk of ventilator-associated pneumonia.

NCT ID: NCT00876252 Completed - Clinical trials for Pneumonia, Ventilator-Associated

Study Assessing Immunogenicity and Safety of IC43 In Intensive Care Patients

Start date: December 2008
Phase: Phase 2
Study type: Interventional

Randomized, placebo-controlled, partially blinded phase 2 pilot study. Multicenter study (approximately 50 centers) in approximately 9 countries. Proposed start date is December 2008. The study duration per patient is estimated to be 90 days. Overall study duration is estimated to be 12-18 months.

NCT ID: NCT00861315 Recruiting - Clinical trials for Ventilator Associated Pneumonia

Pharmacokinetics of Nebulized Amikacin in Patients With Pneumonia Undergoing Mechanical Ventilation

DARTAGNAN
Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Inclusion of patients undergoing mechanical ventilation and presenting a pneumonia in order to determine serum pharmacokinetics of nebulized amikacin. The primary aim is to determine the dose of amikacin to be nebulized in order to observe amikacin serum concentrations close to but inferior to those observed after standart intravenous amikacin infusion.

NCT ID: NCT00851435 Completed - Pneumonia Clinical Trials

Safety and Pharmacokinetics of KBPA-101 in Hospital Acquired Pneumonia Caused by O11 Pseudomonas Aeruginosa

Start date: February 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The objectives of this open study are to assess the safety, tolerability, pharmacokinetics and clinical outcome of patients who have HAP caused by Pseudomonas aeruginosa serotype O11 after three separate administrations of KBPA-101 every third day in addition of standard of care antibiotic treatment.

NCT ID: NCT00842478 Recruiting - Pneumonia Clinical Trials

Effectiveness of Dental Brushing for Preventing Ventilator-Associated Pneumonia

RASPALL
Start date: May 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Poor oral hygiene is associated with respiratory pathogen colonization and secondary lung infection.The possible association between oral care and incidence of VAP, and the role of dental plaque, mouth and tracheal colonization have not been firmly established. The investigators' hypothesis was that improving oral care with electrical toothbrushing might be effective in reducing the incidence of VAP.

NCT ID: NCT00829842 Completed - Clinical trials for Ventilator Associated Pneumonia

Oral Hygiene With Chlorhexidine and Incidence of Ventilator-Associated Pneumonia in Children Submitted to Heart Surgery

Start date: February 2006
Phase: Phase 3
Study type: Interventional

Hospital infections play an important role in the increase of patients' morbimortality and hospitalization costs, especially in the case of individuals admitted to intensive care units (ICU) during postoperative heart surgery. Analysis of the epidemiological profile of the hospital infections in the pediatric-ICU (P-ICU) of Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto, University of São Paulo (HCFMRP-USP) demonstrated a 31.1% incidence of pneumonia (PNM) and a rate of ventilator-associated pneumonia (VAP) of 23.81 per 1000 ventilators-day between March 2004 and February 2005 in the group submitted to cardiac surgery. Knowledge of the pathophysiology and risk factors associated with this infection allows for measures aiming at reducing its incidence. The objective of the present study is to evaluate the effect of oral hygiene with a 0.12% chlorhexidine solution on the incidence of PNM and PAV in children submitted to cardiac surgery.

NCT ID: NCT00786305 Completed - Pneumonia Clinical Trials

Nebulized Ceftazidime and Amikacin in Ventilator Associated Pneumonia

Start date: October 2004
Phase: Phase 2
Study type: Interventional

Pseudomonas aeruginosa is one of the major causative microorganisms of ventilator-associated pneumonia often resistant to antibiotics. In experimental models, nebulization of antibiotics delivers high lung tissue concentrations of antibiotics in infected lungs and increases lung bacterial killing. The aim of the study is to assess the efficiency of nebulized ceftazidime and amikacin in the treatment of pneumonia caused by Pseudomonas aeruginosa in ventilated patients.