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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT03011853 Completed - Critical Care Clinical Trials

Survival After Failed First-line Non-invasive Ventilation in Acute on Chronic Obstructive Pulmonary Disease

Start date: January 2008
Phase:
Study type: Observational [Patient Registry]

Observational cohort study of mid-to-long term survival of patients with acute on chronic obstructive pulmonary disease, analyzed per type of ventilation support provided during first 24 hours in intensive care.

NCT ID: NCT03011515 Completed - Pneumonia Clinical Trials

Evaluating a Host-response Based Diagnostic for Distinguishing Between Bacterial and Viral Etiology in Patients With Lower Respiratory Tract Infection (LRTI)

OBSERVER
Start date: March 10, 2017
Phase:
Study type: Observational

The purpose of this study is to validate the diagnostic accuracy of a novel host-response based diagnostic tool for differentiating between bacterial and viral etiologies in adult patients aged 18 years and older with clinical suspicion of lower respiratory tract infections (LRTI)

NCT ID: NCT03010592 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Studying the Airway Microenvironment in Patients Undergoing Surgical and Bronchoscopic Interventions for COPD

COPD-ENVIRON
Start date: February 6, 2017
Phase:
Study type: Observational

Studying the airway microenvironment in patients undergoing surgical and bronchoscopic interventions for COPD

NCT ID: NCT03010566 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Lung Volume Reduction Coil Microbiome Study

LVRC-Micro
Start date: January 30, 2017
Phase:
Study type: Observational

Studying the microbiome of the lung in patients treated with endobronchial lung volume reduction coils for emphysema

NCT ID: NCT03010449 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

LVR in Severe Emphysema Using Bronchoscopic Autologous Blood Instillation in Combination With Intra-bronchial Valves

BLOOD-VALVES
Start date: August 24, 2017
Phase: N/A
Study type: Interventional

A single arm pilot study of lung volume reduction in severe emphysema using bronchoscopic autologous blood instillation in combination with intra-bronchial valves.

NCT ID: NCT03008915 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Targeting Pulmonary Perfusion in Alpha-1 Antitrypsin Deficiency

Start date: January 2017
Phase: Phase 2
Study type: Interventional

The aim of this study is to test whether aspirin improves endothelial function in alpha-1 antitrypsin deficiency-associated lung disease, measured by pulmonary microvascular blood flow on magnetic resonance imaging (MRI) and with apoptotic endothelial microparticles.

NCT ID: NCT03008746 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Pulmonary Microbiota in Patients With Chronic Obstructive Pulmonary Disease Colonized With P. Aeruginosa Resistant to Imipenem

MiPAD
Start date: January 12, 2017
Phase: N/A
Study type: Interventional

Pseudomonas aeruginosa (PA ) is associated with chronic lung infections in patients with chronic obstructive pulmonary disease (COPD). Commensal flora (microbiota) in lung was recently described using high-throughput sequencing techniques (NGS). PA strains isolated during lung infection episodes of severe COPD patients often show resistance to antibiotics including imipenem that is mainly due to mutation in oprD. In collaboration with Harvard Medical School, the investigators have recently demonstrated that PA OprD mutant shows increased survival (fitness) and its virulence. This bacterium could be more likely to colonize. Colonization by PA OprD mutant could influence the pulmonary microbiota and may worsen disease evolution, particularly in terms of frequency of exacerbations. Our objective is to describe modification of pulmonary microbiota associated with PA colonization, including OprD PA mutant, in severe COPD patients. The investigators will correlate the microbiota modification to medical history. Stable severe COPD patients will be included. Three groups of patients will be sampled: 1) not PA colonized, 2) PA colonized and 3) PA OprD mutant colonized. Medical history will be recorded by the physician as usual and three samples will be performed: 1) sputum, 2) oral wash and 3) water used for oral wash. Regular bacterial culture will be performed and NGS will be performed also to characterize the microbiota.

NCT ID: NCT03004716 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Telemonitoring in Pulmonary Rehabilitation: Validity of a Remote Pulse Oxymetry System

TELE-REHAB
Start date: January 2017
Phase: N/A
Study type: Observational

The purpose of this study is to assess the feasibility and the reliability of a telemonitoring system during pulmonary rehabilitation in patients with chronicle obstructive pulmonary disease. The feasibility is assessed using the patient's satisfaction and it ease of use. The reliability of the remote telemonitoring system is assessed comparing the local data (extracted from the monitoring device itself) and the data transmitted through the telemonitoring platform.

NCT ID: NCT03004352 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Disturbed Blood Flow Induces Endothelial Dysfunction in Severe Chronic Obstructive Pulmonary Disease

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

The aim of the study is to determine if increased retrograde shear would further deteriorate the already impaired vascular function in severe COPD patients.

NCT ID: NCT03003559 Recruiting - COPD Exacerbation Clinical Trials

HFNC vs Nasal Cannula in Mild Chronic Obstructive Pulmonary Disease Exacerbation

Start date: January 2017
Phase: N/A
Study type: Interventional

For AECOPD patients, only 8% patients ventilated by noninvasive and invasive positive pressure ventilation. Nasal cannula is the most common pattern of oxygen therapy in mild AECOPD. As a low flow oxygen therapy, nasal cannula has many disadvantages.Therefore, we design a randomized controlled trial(RCT)to explore whether HFNC would be better than nasal cannula to prevent the aggravation of respiratory failure and endotracheal intubation in mild AECOPD.