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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT02512510 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Efficacy Study of Nebulized TD-4208 for Chronic Obstructive Pulmonary Disease (COPD)

COPD
Start date: September 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to measure the effectiveness and safety of TD 4208, an investigational drug being developed to treat people with moderate to very severe COPD, compared to placebo, a treatment without activity.

NCT ID: NCT02512302 Completed - COPD Clinical Trials

Study to Determine the Amount of Glycopyrrolate Absorbed in the Lungs After Taking the Medicine With a eFlow Nebulizer and Seebri® Breezhaler® With and Without Activated Charcoal in Subjects With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD).

GOLDEN7
Start date: October 2015
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to determine the amount of medicine absorbed in the lungs following dosing via eFlow nebulizer and Seebri® Breezhaler® with and without activated charcoal in subjects with moderate to severe chronic obstructive pulmonary disease (COPD).

NCT ID: NCT02506504 Completed - Clinical trials for Obstructive Lung Diseases

Prevention of Post-exercise Muscle Fatigue and Effect on Exercise Training in Severe Patients With COPD.

QUADRIVEND
Start date: June 25, 2014
Phase: N/A
Study type: Interventional

In patients with severe Chronic Obstructive Pulmonary Disease (COPD), exercise tolerance is severely impaired due to a ventilatory limitation, levelling off the intensity of exercise. This reduces the physiological benefit of pulmonary rehabilitation. In these patients, it is then proposed to add an Inspiratory Pressure Support (IPS) in order to increase the intensity and the duration of every training session. In a preliminary study, the investigators showed that IPS applied during an exhaustive cycling exercise allowed to prevent the onset of post-exercise quadriceps fatigue evaluated by the endurance time to isotonic quadriceps contractions (TlimQ). The aim of this study is to determine the relationship between the prevention of post-exercise fatigue (TlimQ) and the change in training load (intensity x time x number of sessions) during a pulmonary rehabilitation programme. At the beginning of the training programme, 25 patients will be evaluated for TlimQ after a cycling exercise (70% maximal workload) with and without IPS in random order. The training load was then monitored at every exercise session of the programme.

NCT ID: NCT02504814 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Physiological and Clinical Changes in NHF Therapy

ATMOFLOW
Start date: June 2011
Phase: N/A
Study type: Interventional

The study explores the changes in pressure, volume and in hypercapnia in patients with COPD and ILD. The investigators will use different application forms.

NCT ID: NCT02502201 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Environment Effect on Six-Minute Walk Test Performance

6MWTAATD
Start date: October 2015
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine the effect of the environment on six-minute walk test performance in individuals with chronic obstructive pulmonary disease due to alpha-1 antitrypsin deficiency. The aim of the study is to determine the environmental impact on physical performance in this population to determine if any factors influence quality of life. This study was developed to evaluate the efficacy of the using the indoor six-minute walk test to determine eligibility for ambulatory oxygen therapy.

NCT ID: NCT02499718 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Non-invasive Positive Pressure (NPPV ) for Severe Stable Chronic Obstructive Pulmonary Disease

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

Assessment of the effect and safety of noninvasive positive pressure ventilation for severe stable chronic obstructive pulmonary disease

NCT ID: NCT02499653 Recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Psychological Intervention to Promote Acceptance and Adherence to NIV in People With COPD

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

This study aims to analyze the impact of a brief psychological support intervention in the promotion of the adherence to Non Invasive Ventilation (NIV) among people with Chronic Obstructive Pulmonary Disease (COPD). The investigators expect to see a positive impact of this intervention on both physical and psychological well-being, and consequently, a reduction of health costs.

NCT ID: NCT02499068 Completed - COPD Clinical Trials

Madrid Project on the Management of Chronic Obstructive Pulmonary Disease With Home Telemonitoring

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

The purpose of the study is to verify the clinical effectiveness of a managed home telemonitoring program in patients with severe COPD against usual clinical practice, as measured by the decrease in the number of exacerbations, number of hospitalizations, hospital days and emergency room visits in a 12 month period The primary endpoint of effectiveness is "severe exacerbations avoided." The main hypothesis is that patients with severe or very severe COPD patients managed with a home telehealth program have better outcomes than patients managed according to usual clinical practice.

NCT ID: NCT02498496 Withdrawn - Clinical trials for Pulmonary Disease, Chronic Obstructive

Magnesium Sulfate to Prevent Hospitalisation of Acute Exacerbations of Chronic Obstructive Pulmonary Disease

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

The purpose of this study is to assess whether administration of a bolus dose of MgSO4 (magnesium sulfate) plus standard therapy is superior to standard therapy alone for the management of Acute Exacerbations of Chronic Pulmonary Obstructive Disease (AECOPD) in the emergency department. The investigators hypothesize that MgSO4 causes faster recovery of the bronchospasm, and a reduction of the dead space, translating to the following clinical outcomes : less hospitalisation, lower length of stay (LOS), better composite outcome of hospitalisation + LOS + readmission for AECOPD.

NCT ID: NCT02493790 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Cognitive Dysfunction in COPD Patients : Role in the Performance of Cognitive-motor Dual Task Situation?

DysCo
Start date: October 2014
Phase: N/A
Study type: Observational

Chronic Obstructive Pulmonary Disease (COPD) is a respiratory disease starting point characterized by multiple systemic effects as cognitive dysfunction. This one seems to have an impact in activity daily living, considered mainly as a cognitive-motor dual task situations. Yet to date, no study has specifically focused in the cognitive-motor performance in patients with COPD or on the effects during a rehabilitation program. The main objective of this work was to evaluate the impact of cognitive dysfunction in COPD, comparing performance between COPD patients and healthy subjects in a single and dual task cognitive-motor situation. The secondary objective was to assess the impact of a rehabilitation program on these performances.