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Emphysema clinical trials

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NCT ID: NCT02100800 Completed - Emphysema Clinical Trials

Assessment of Emphysema Using 1.5T MRI With UTE Pulse Sequences

EMPHYREM
Start date: May 23, 2014
Phase: N/A
Study type: Interventional

Emphysema is a major pathological feature of Chronic Obstructive Pulmonary Disease (COPD). Non-invasive assessment of emphysema is a crucial issue for the phenotype and follow-up of COPD patients. Currently, CT is the method of reference to evaluate and quantify emphysema but it remains a radiation-based technique. Magnetic Resonance Imagery (MRI) with ultrashort echo time (UTE) pulse sequences is a promising non-ionizing alternative for lung imaging. Our objective is to evaluate emphysema in COPD patients using CT and MR-UTE, and to test the agreement between both techniques.

NCT ID: NCT02099799 Completed - COPD Clinical Trials

The Effect of Physical Activity Promotion on Short and Long-term Outcomes in COPD

WEB
Start date: November 17, 2015
Phase: N/A
Study type: Interventional

COPD currently afflicts 24 million US residents; the prevalence of COPD is high among Veterans. Persons with COPD have significant functional disability as a result of the disease. This project will determine whether a novel Internet-mediated walking program coupled with a pedometer can improve exercise capacity, improve health-related quality of life, and decrease the risk of acute exacerbations in persons with COPD. If successful, based on estimates that 33 to 64% of COPD patients are Internet users, the proposed exercise intervention could help over 8 million persons. The Veterans Health Administration (VHA) has a strong commitment to providing care to persons with COPD and supporting research directed at COPD-related disability. The 2012-2016 Strategic Plan of the VHA Office of Research and Development includes research in COPD rehabilitation. The proposed research addresses Rehabilitation R&D Service's current priority area of improving disabled Veterans' health-related quality of life by reducing disease burden and maximizing functional recovery.

NCT ID: NCT02059057 Terminated - Emphysema Clinical Trials

LVRC IDE Crossover Study (Crossover From IDE Trial CLN0009)

CROSSOVER
Start date: December 2013
Phase: N/A
Study type: Interventional

Crossover study for patients who were randomized to the Control Group in CLN0009 (NCT01608490).

NCT ID: NCT02056158 Completed - HIV Clinical Trials

HIV+ Alveolar Macrophage Oxidant-mediated Apoptosis of Pulmonary Endothelium

Start date: January 13, 2014
Phase:
Study type: Observational

In HIV+ cigarette smokers, with no prior history of pulmonary infections, emphysema is often developed at an earlier age and is a significant cause of morbidity despite treatment with antiretroviral drugs. Preliminary data gathered from HIV+ individuals that smoke cigarettes strongly support the hypothesis that the combination of HIV infection and smoking creates increased stress in the lower respiratory tract. To examine the underlying factors that contribute to the accelerated development of emphysema in this cohort, samples from the lower respiratory tract will be provided by HIV+ and HIV- subjects. The samples collected will serve as biomarkers for assessing the onset of emphysema.

NCT ID: NCT02042976 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Mindfulness-based Cognitive Therapy for Chronic Obstructive Pulmonary Disease

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

The purpose of the study is to determine the efficacy of mindfulness-based cognitive therapy (MBCT) as an add-on to pulmonary rehabilitation (treatment as usual, TAU) in chronic obstructive pulmonary disease (COPD). The investigators hypothesize that compared to treatment-as-usual, the add-on of MBCT will result in improved psychological (anxiety, depression) and physical outcomes (physical health status, activity level, inflammatory markers). Furthermore, the investigators will explore the possible moderating role of individual differences in sociodemographic and disease-related characteristics and the perceived quality of the therapeutic alliance, as well as the mediating role of mindfulness, breathlessness catastrophizing, self-efficacy, and self-compassion for the hypothesised effect.

NCT ID: NCT02025205 Completed - Clinical trials for Endoscopic Lung Volume Reduction With Endobronchial Valve

Improving Patient Outcomes by Selective Implantation of the Zephyr EBV - Study

IMPACT
Start date: August 2014
Phase: N/A
Study type: Interventional

The aim of this prospective, randomized, controlled, one-way crossover study is to assess and compare the efficacy of the Zephyr endobronchial valves vs. Standard of Care (SoC) in patients suffering from COPD with Homogeneous Emphysema. Patients will be followed up for 12 months after randomization. Patients in the SoC arm will crossover to the EBV treatment arm after the 6-month visit and will be followed up for 6 additional months.The primary objective is the variation of FEV1 between baseline and 3-month follow-up visit. The secondary objectives will evaluate quality of life, exercise capacity, dyspnea (including BODE index) changes, target lobe volume reduction, as well as safety outcomes.

NCT ID: NCT02022683 Completed - COPD Clinical Trials

To Improve Lung Function and Symptoms for Emphysema Patients Using Zephyr Valves

TRANSFORM
Start date: January 28, 2014
Phase: N/A
Study type: Interventional

To compare the clinical outcomes of Endoscopic Lung Volume Reduction (ELVR) using Pulmonx Zephyr Valves vs. Standard of Care (SoC) in the treatment of heterogeneous emphysema subjects in a controlled trial design setting.

NCT ID: NCT02012673 Completed - COPD Clinical Trials

A Safety and Feasibility Study of Re-treating Patients With Severe Emphysema With the RePneu LVRC System.

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

Rationale: The combined data from 3 studies outside the Unites States investigating the Lung Volume Reduction Coil system (RePneu LVRC) showed statistically significant improvements in pulmonary function, exercise capacity and quality of life at both 6-Months and 12-Months post treatment. 24 months post treatment the improved pulmonary function and exercise capacity are slightly decreasing. Retreating the patient with the LVR coil system in other parts of the lung could potentially lead to new improvements in lung function, dyspnea, exercise capacity and quality of life and may reduce the rate of decline. Objective: To investigate the safety and feasibility of re-treating patients with severe Chronic Obstructive Pulmonary Disease (COPD) with the RePneu LVRC system.

NCT ID: NCT02008162 Recruiting - COPD Clinical Trials

Bronchoreversibility and Radiologic Morphology of Emphysema

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

To assess response to bronchodilation with tiotropium plus salbutamol in patients with severe emphysema and analyze relationships between bronchoreversibility response and semiquantitative computed-tomography based emphysema severity measures.

NCT ID: NCT02006576 Completed - Emphysema Clinical Trials

Prostaglandin Inhibition for Emphysema

PIE
Start date: January 1, 2014
Phase: Phase 2
Study type: Interventional

The Prostaglandin Inhibition for Emphysema (PIE) study will determine if a currently available therapy, ibuprofen 600 mg three times daily, can block PGE production in the lower respiratory tract and if this results in improvement in measures of lung repair function.