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Ventilator Associated Pneumonia clinical trials

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NCT ID: NCT05258682 Not yet recruiting - COVID-19 Clinical Trials

Safety of Nebulized Combination Therapy BromAc® in COVID-19 Respiratory Disease

Start date: May 1, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

COVID-19 has multiple facets including cytokine storm, thromboembolism and gelatinous secretions. It is known that oxygen exchange is the main problem in patients with COVID-19 and hypoxia is one of the most serious, in which patients succumb to acute respiratory distress syndrome (ARDS). In other severe respiratory disease such as ventilator associated pneumonia (VAP), formation of biofilm in the endotracheal tube causes infection to spread to the lungs, resulting in respiratory decline and high mortality. The development of gelatinous sputum plugs correlates with negative outcome. Both groups of patients still have limited therapy options. BromAc is a potent mucolytic, biofilm degrader, cleaves the glycoproteins of the SARS-CoV-2 virus (antiviral), and down regulates cytokines and chemokine in COVID-19 sputum. The investigators seek to examine the safety and attempt to gain preliminary efficacy of nebulised BromAc in moderate to severe COVID-19 and other mucus producing, severe, respiratory diseases.

NCT ID: NCT04903886 Not yet recruiting - Bacteremia Clinical Trials

Intensive Care Unit Acquired Infections in Patients Colonized With Extended Spectrum Enterobacteriaceae

BMREA
Start date: June 1, 2021
Phase:
Study type: Observational

Worldwide emergence of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) had become a major problem in ICU, with at least 10% of incidence at the admission in Europe. A systematic rectal swab is used in 70% of French ICU to detect intestinal ESBL-E carriage The relationship between intestinal carriage and ICU-acquired infection is not perfectly known. The investigators conducted a five years study monocentric retrospective observational cohort in patients with presence of extended-spectrum β-lactamase-producing Enterobacteriaceae in systematic rectal swabs to investigate which type of infections and which bacteria are involved. The investigators also collect data about antibiotherapy used to treat these infections.

NCT ID: NCT04344509 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Microbial Etiology of Ventilator-associated Pneumonia in COVID-19 Infected Patients

Start date: June 2020
Phase:
Study type: Observational

National multicentric observational retrospective case-control study comparing the relative frequency of the various microorganisms responsible for VAP in patients infected or not by SARS-CoV-2 and their resistance to antibiotics.

NCT ID: NCT04111224 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Evaluation of pentraxin3 as a Marker for Ventilator Associated Pneumonia

Start date: February 1, 2020
Phase:
Study type: Observational

This study will assess the role of pentraxin3 (PTX3) in the early diagnosis of ventilator-associated pneumonia (VAP) and the detection of antibiotic sensitivity for different organisms isolated from tracheal aspirate.

NCT ID: NCT04057625 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Transthoracic Ultrasound in the Diagnosis and Follow-up of Ventilator Associated Pneumonia

Start date: September 2019
Phase: N/A
Study type: Interventional

To evaluate the sensitivity, specificity and diagnostic accuracy of bedside transthoracic ultrasound examination in the diagnosis and follow up of ventilator associated pneumonia.

NCT ID: NCT03871985 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Efficacy of Two Intermittent Subglottic Secretion

Start date: March 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of intermittent subglottic secretion lavage combined with aspiration preventing ventilator associated pneumonia in patients with severe neurological disease

NCT ID: NCT03294837 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Treatment of Ventilator Associated Pneumonia in Pediatric Intensive Care Unit

Start date: November 2017
Phase: N/A
Study type: Observational

treatment of ventilator associated pneumonia in pediatric intensive care unit according to the American guidelines

NCT ID: NCT03267693 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Gastrointestinal Complications in Association With Oropharyngeal and Respiratory Infections in Mechanical Ventilation

Start date: September 2017
Phase: N/A
Study type: Observational

Detection of gastrointestinal complications in mechanically ventilated critically ill patients and its relation to oropharyngeal and respiratory infections in relation to oropharyngeal and gastric PH.

NCT ID: NCT03266380 Not yet recruiting - Clinical trials for Ventilator Associated Pneumonia

Risk Factors and Common Preventive Measures for Ventilator Associated Pneumonia in Patients With Severe Traumatic Brain Injury

Start date: January 1, 2018
Phase: N/A
Study type: Observational

The primary objective of this study is to assess the incidence of VAP in patients with TBI and to identify risk factors for developing VAP in this specific patient population (types of co-injuries in patients with multiple trauma or characteristics on admission). The secondary objective is to assess the prevalence of pathogens responsible for early- and late-onset VAP in patients with TBI. The tertiary objective is to discuss the ability of preventive measures to reduce the incidence of VAP

NCT ID: NCT03018431 Not yet recruiting - Clinical trials for Ventilator-Associated Pneumonia

CT Scan and Lung Ultrasonography to Improve Diagnostic of Ventilation Acquired Pneumonia in ICU

ECTOPICUS
Start date: October 15, 2017
Phase: N/A
Study type: Observational [Patient Registry]

We aim to show that systematic ultrasonography performed in ventilated patients suspected of ventilation-acquired pneumonia could improve the accuracy of diagnostic of pneumonia, and helps defining the diagnostic of tracheobronchitis when lower respiratory tract infection is considered. Chest CT scan is often performed before or just after admission in ICU, and usually show abnormalities that are revealed later on standard radiographs. This last exam is traditionally considered as the gold standard to prove new pulmonary infiltrates, but the correlation with parenchymal consolidation is pretty low, and lead to over-diagnosing pneumonia, thus leading to a massive and maybe sometimes unconsidered prescription of antibiotic therapy. Lung ultrasonography conducted systematically within the 3 first days after suspcion of pneumonia could help making the difference between real infection-linked lesions, and banal abnormalities following the hydric inflation of intra-thoracic organs, for instance pulmonary edema or pleural effusion. An independent evaluation using lung ultrasound, and analysis of CT scan acquisition when performed, compared with the physician in charge of the patient appreciation by suggesting him to provide his own probability of pneumonia upon routine clinical and biological datas.