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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT01762917 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Influence of Bag Volume Variation on the Reproducibility of Inert Gas Rebreathing

Start date: September 2007
Phase: N/A
Study type: Observational

Non-invasive inert gas rebreathing (IGR) based on the Fick Principle showed promising results in the determination of pulmonary blood flow (PBF). The volume of the rebreathing bag (Vbag) is proposed by the system, however, elderly patients or those suffering from high grade pulmonary diseases might be unable to entirely rebreathe this volume and therefore fail to completely mix the test gases. The aim of our study is to evaluate the effect of adapting Vbag on the reproducibility of IGR measurements in patients with obstruction (group A), restriction (group B) and pulmonary healthy controls (group C).

NCT ID: NCT01759199 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Six-minute Stepper Test as an Outcome Measure of Exercise Tolerance During Pulmonary Rehabilitation in With Chronic Obstructive Pulmonary Disease (COPD) Patients(STEPPER)?

STEPPER
Start date: September 2012
Phase: N/A
Study type: Interventional

The aim of this study is to show if the six-minute stepper test (ST6) is a sensible marker of exercise tolerance evolution during a pulmonary rehabilitation program in people with all stages of severity of Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT01754844 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

A First Time in Man Study to Asses the Safety and Tolerability of AZD7624 in Healthy Subjects

Start date: January 2013
Phase: Phase 1
Study type: Interventional

This is a First in Human study to assess the safety and tolerability of AZD7624, following inhaled administration of single ascending doses in healthy male volunteers and female volunteers of non-child bearing potential. Pharmacokinetics (what the body does to the drug) and pharmacodynamic (what the drug does to the body) parameters will be also assessed as secondary objectives.

NCT ID: NCT01753427 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Perception of Symptom Variability in COPD

Start date: December 2012
Phase: N/A
Study type: Observational

The objective of the study is to assess patient's perception with stable state COPD on symptom variability and to describe how symptom variability impacts daily quality of life in Chinese COPD patient with moderate, severe or very severe airflow limitation from tier 3 hospitals in China where most of COPD patients are diagnosed and treated.

NCT ID: NCT01750658 Completed - COPD Clinical Trials

Study of Chronic Obstructive Pulmonary Disease (COPD) Exacerbations In Spain

ECOS
Start date: September 2006
Phase: N/A
Study type: Observational

ECOS is a cross-sectional, observational, longitudinal, multicenter study enrolling 100-200 patients during a COPD exacerbation.

NCT ID: NCT01750489 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Muscle Dysfunction in Patients With Chronic Obstructive Lung Disease (COPD): the Role of Sympathetic Activation

Start date: August 2011
Phase: N/A
Study type: Interventional

The objective of the project is to better understand the causes of exercise limitation, dyspnea and neurohumoral activation in patients with COPD. In particular, the investigators aim to explore the mutual interaction of neurohumoral activation and exercise limitation thereby focussing on differential effects of the peripheral muscle and the diaphragm. Eventually the findings might influence treatment modalities. If sympathetic activation contributes to exercise limitation then drugs influencing the autonomic nervous system would be a reasonable therapeutic concept. If a reduction of sympathetic activity due to an alteration of the ergoreflex can be achieved by non-invasive ventilation this would help to improve dyspnea and exercise capacity.

NCT ID: NCT01749462 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Oxis 9mcg Turbuhaler Clinical Experience Investigation

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

The purpose of the investigation is to confirm the ADR development and the contributing factors possibly having an impact on the safety under the post-marketing actual use of Oxis 9 mcg Turbuhaler.

NCT ID: NCT01744093 Completed - HIV Clinical Trials

Doxycycline for COPD in HIV-Infected Patients

Start date: December 8, 2014
Phase: N/A
Study type: Interventional

In the context of improved survival from HIV infection itself, chronic obstructive pulmonary disease (COPD); a form of lung disease that includes emphysema, which makes breathing difficult) is emerging as an important cause of morbidity and perhaps ultimately mortality in this population. HIV-infected patients are at increased risk of chronic obstructive pulmonary disease, likely due to multiple factors, including an increased presence of smoking, chronic inflammation and progression of immunodeficiency, oxidant stress (excessive levels of natural chemicals called oxidants and free radicals that can damage tissue), and respiratory infections. While natural history data on COPD are limited in the era of potent antiretroviral therapy, earlier data suggest that the course of emphysema may be accelerated in this population. Our preliminary data suggest that several matrix metalloproteinases (MMPs) derived from alveolar macrophages (a type of immune cell found in the lungs) have an increased cellular response in HIV-infected smokers, which could contribute to accelerated emphysema. Matrix metalloproteinases are enzymes that break down the structural support of tissues, including the airways in the lung. Based on these observations, the investigators hypothesize that pharmacologic inhibition of matrix metalloproteinases by doxycycline will favorably modify the natural history of chronic obstructive pulmonary disease in HIV-infected patients. To test this hypothesis, the investigators propose conducting a proof of concept pilot study as a prelude to a possible phase II randomized, placebo-controlled trial (testing safety and efficacy in a larger population controlled with a "sugar pill") of doxycycline for COPD in HIV-infected patients should the proof of concept be successful. Our research team is lead by a pulmonologist/researcher with expertise in HIV-associated COPD and an infectious diseases specialist/clinical trials expert.

NCT ID: NCT01744028 Completed - Clinical trials for Remote Patient Monitoring in COPD Patients

Compare the Effect of a Remote Monitoring System Using the EXACT Tool to Reduce Hospitalizations Due to Chronic Obstructive Pulmonary Disease (COPD) Exacerbations. EXACT = Exacerbations of Chronic Pulmonary Disease Tool.

PREMIERE
Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this pilot study is to evaluate a remote patient monitoring (RPM) system using a daily PRO tool (EXACT = Exacerbations of Chronic Pulmonary Disease Tool), in preventing hospitalization from Chronic Obstructive Pulmonary Disease (COPD) exacerbations in a COPD population at high risk of exacerbation, compared to those managed by usual care.

NCT ID: NCT01741480 Completed - Cancer Clinical Trials

Early Warning System

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

The study will begin in 2013 whereby patients having an early warning system (EWS) alert will be randomized to be seen by the rapid response team (RRT) for triage versus usual care. A RRT is usually made up of a nurse and/or a physician who respond to a requested activation of the RRT (called an "ACT"). The intervention will occur as follows: