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Lung Diseases clinical trials

View clinical trials related to Lung Diseases.

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NCT ID: NCT02864342 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD

Adherence Study in COPD Patients

Start date: August 12, 2016
Phase: Phase 4
Study type: Interventional

A randomized clinical study to assess the impact of Symbicort® pMDI medication reminders on adherence in COPD patients

NCT ID: NCT02862418 Recruiting - Pulmonary Disease Clinical Trials

Imaging of Lungs With a New Type of Magnetic Resonance Imaging (MRI) Called UTE (Ultrashort Echo Time)

Start date: October 2015
Phase:
Study type: Observational

This research study has 2 purposes: 1. To learn about new ways to use Magnetic Resonance Imaging (MRI) to take clearer pictures of the lungs. A type of MRI called Ultra Short Echo Time (UTE) will be used as well as traditional MRI. 2. To collect images and health information about lungs that have different kinds of lung diseases to compare to healthy lungs. This collection will help researchers and clinicians to better understand lung variations in health and disease. This study will involve one MRI session that will take about 10 to 30 minutes and for some participants a breathing test that measures how well the lungs are working. This test is called spirometry.

NCT ID: NCT02860728 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Resistance Training to Prehabilitate Patients With Chronic Obstructive Pulmonary Disease

Start date: August 2016
Phase: N/A
Study type: Interventional

Structural changes in skeletal muscles of patients with chronic obstructive pulmonary disease (COPD) have been linked to impaired muscle function, reduced exercise capacity, and increased mortality associated with this disease. Muscle dysfunction also contributes to dyspnea intensity and the ability to sustain exercise, making aerobic exercise training intolerable at the intensity and/or volume required to achieve clinically important changes. Resistance training (RT) is an attractive exercise modality because it is efficacious and more tolerable initially. No work has examined whether a short-term RT program can reduce exertional symptoms and improve exercise tolerance (dyspnea and leg fatigue) in patients with COPD.

NCT ID: NCT02859194 Completed - Bronchiectasis Clinical Trials

The Effect of Lt to Rt Shunt Using Veno-veno-arterial Extracorporeal Membrane Oxygenation (ECMO) on Coronary Oxygenation in Lung Transplantation Patients

Start date: May 31, 2016
Phase: N/A
Study type: Interventional

ECMO(Extracorporeal membrane oxygenation) is being essential for cardiopulmonary failure patients. There are two types of ECMO, which is veno-veno (V-V) that can be used in respiratory failure patients and veno-arterial (V-A) that can be used in cardiac failure patients. V-A ECMO can also be used during lung transplantation, substitution of cardiopulmonary bypass, which can show sufficient performance during operation and better postoperative outcome. However, regarding V-A ECMO circulating from femoral vein to femoral artery, there is a pro blem of differential hypoxia which might influence coronary artery and head vessels. In this prospective study, the investigators are planning to put another ECMO catheter into internal jugular vein which takes a role of left to right shunt, to mitigate the hypoxia of coronary artery.

NCT ID: NCT02858791 Completed - Clinical trials for Pulmonary Hypertension

MIF- Thyroxine Interactions in the Pathogenesis of Pulmonary Arterial Hypertension

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

The investigators will investigate the interrelationship of macrophage migration inhibitory factor (MIF) and free T4 in patients with PAH.

NCT ID: NCT02858180 Completed - Heart Failure Clinical Trials

Hepatitis C Virus(HCV) Heart and Lung Study

Start date: December 2016
Phase: Phase 4
Study type: Interventional

This is a multicenter study in Hepatitis C Virus (HCV) infected adult patients who also have advanced cardiac disease or advanced lung disease.

NCT ID: NCT02857842 Completed - COPD Clinical Trials

Corticosteroid Reduction in COPD

Cortico-cop
Start date: August 2016
Phase: Phase 4
Study type: Interventional

This study explores whether patients hospitalized with chronic obstructive pulmonary disease (COPD) exacerbation may have fewer days with prednisolone and with the same treatment effect by controlling the treatment by daily measurements of eosinophils.

NCT ID: NCT02854280 Completed - Healthy Volunteers Clinical Trials

Brain During Effort : Effects of Hypoxia With Respiratory Patients

NEUROX
Start date: June 2013
Phase: N/A
Study type: Interventional

Brain oxygenation is determined by the product of CaO2 and the cerebral blood flow (CBF), the modification of one or the other can affect the neuronal O2 availability. Besides the effect of the PaO2, the CBF is also regulated by the PaCO2. During effort in state of hypoxia, the drop of the PaO2 associated to a potential decrease of the PaCO2 and therefore of the CBF, can create an important dizziness between the demand and the supply of cerebral O2. It seems that hypoxia can trouble in a significant way the response of central neurons, just as the production of a motor cortex generated motor command. Studies suggest that exercise in severe hypoxia condition can constitute a necessary threat for brain oxygenation and the motor command, with the consequence a decrease of the exercise performance. This projects aim to study effects of hypoxia on the brain function for patients suffering from chronic respiratory disease. Neurophysiologic responses of the brain while resting or exercising, including drip and cerebral oxygenation, cortical excitation and motor command resulting for hypoxic subjects before and after a treatment to correct abnormalities of gaz in blood. The study will use a multidisciplinary and supplementary methodological approach : the near-infrared spectroscopy (NIRS) to appreciate the drip and cerebral oxygenation, CBF, neurostimulation procedures and electromyography (EMG) to appreciate the cortical excitability, measure the level of central activation and motor command. The goals of this study will be : - Measure the drip and cerebral oxygenation, the cortical excitability, mechanisms of voluntary activation and central fatigue to the effort for the chronic hypoxemic patient compared to healthy control subjects. - Analyse disruptions of locomotion parameters and posturographyc, in simple and double task, involving different levels of cerebral task. - Analyse acute effects of an improvement of arterial oxygenation for patients suffering from chronic obstructive pulmonary disease (COPD) on drip and cerebral oxygenation, cortical excitability, mechanisms of voluntary activation and central fatigue. - Evaluate effects of a treatment by continuous positive airway pressure (CPAP) for patients suffering from obstructive sleep apnea (OSA) with the same parameters.

NCT ID: NCT02853383 Recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Registry of COPD Patients From Outpatient Polyclinic Healthcare Institutions of the Russian Federation in Moscow

Start date: December 2016
Phase:
Study type: Observational [Patient Registry]

To describe the clinical profile of COPD patient who is under outpatient surveillance at polyclinic institutions of Moscow (including demographic data (age, gender, ethnicity, occupation), smoking status, disease duration, disease severity grade, distribution by disease phenotype, disease exacerbation rate in the setting of real-life clinical practice).

NCT ID: NCT02853123 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Tiotropium + Olodaterol on Breathlessness in COPD Patients

Start date: September 22, 2016
Phase: Phase 4
Study type: Interventional

The primary objective of the present study is to evaluate the effect of tiotropium + olodaterol fixed dose combination (FDC) compared to tiotropium monotherapy on the intensity of breathlessness during the 3min constant speed shuttle test (CSST). A secondary objective is to explore the relationship between reductions in breathlessness during the 3min CSST and reductions in breathlessness during activities of everyday living as measured by the dyspnea domain of the Chronic Respiratory Questionnaire (CRQ) following bronchodilator therapy.