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Chronic Obstructive Pulmonary Disease clinical trials

View clinical trials related to Chronic Obstructive Pulmonary Disease.

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NCT ID: NCT01175265 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of Breathing Retraining in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Start date: November 2008
Phase: Phase 1
Study type: Interventional

Conventional pulmonary rehabilitation programs improve exercise tolerance, peripheral muscle strength, and health related quality of live but not pulmonary function in patients with chronic obstructive pulmonary disease (COPD). The role of breathing retraining techniques in the rehabilitation of patients with COPD remains unclear. The hypothesis to be tested in this study is that pulmonary function, cardio-pulmonary exercise capacity, health related quality of life and cardiac autonomic modulation of patients with COPD who undergo pulmonary rehabilitation plus breathing retraining will be better than that of patients undergoing a conventional pulmonary rehabilitation.

NCT ID: NCT01173328 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of Pursed-lip Breathing on Exercise Tolerance and Dynamic Hyperinflation in COPD

Start date: March 2007
Phase: N/A
Study type: Interventional

Pursed-lip breathing (PLB) has been advocated to reduce respiratory rate and improve oxygen saturation in patients with chronic obstructive pulmonary disease (COPD) at rest. Although PLB is a strategy that potentially reduces expiratory flow limitation, there are only few studies addressing its effects on exercise. This study aimed to assess the ability of PLB to change the breathing pattern, degree of dynamic hyperinflation (DH) and arterial oxygenation in COPD patients during exercise. Exercise tolerance was evaluated by endurance time and respiratory mechanics was evaluated by forced oscillation technique.

NCT ID: NCT01169727 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Observational Study to Evaluate Health Status of Chronic Obstructive Pulmonary Disease (COPD) Patients in Response to Real-life Treatments in Thailand

Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate health status of uncontrolled Chronic Obstructive Pulmonary Disease (COPD) patients in response to treatments in clinical practice.

NCT ID: NCT01169506 Completed - COPD Clinical Trials

Sublingual Tonometry to Assess Tissue Perfusion in Patients With Chronic Obstructive Pulmonary Disease (COPD)

subton
Start date: August 2009
Phase: N/A
Study type: Interventional

Sublingual positioning of a silicon capillary system is applied. After 15 min, while the individual is in resting position with closed mouth and normal tidal breathing through the nose is performed, the silicon capillary system is connected to a capnometer and CO2 tension is measured. The investigators hypothesis is that this setup offers a non-invasive assessment of ventilatory efficiency with similar accuracy as arterial PCO2.

NCT ID: NCT01168310 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

A Trial to Assess the Pharmacodynamic Response in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

Start date: August 2010
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, multi-dose, parallel group trial which will assess the pharmacodynamic response of fluticasone propionate and formoterol fumarate in subjects with COPD.

NCT ID: NCT01167283 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Electrostimulation in Chronic Obstructive Pulmonary Disease (COPD)

ExaEMS2005
Start date: July 2006
Phase: N/A
Study type: Interventional

This study was designed to test the following hypothesis: To investigate whether COPD muscles can respond to stimuli in terms of changes in fiber-type distribution.

NCT ID: NCT01154400 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Hydrolyzed Casein and Whey Protein Supplementation and the Addition of Leucine to Induce Protein Anabolism in Malnourished COPD Patients

Start date: May 2009
Phase: N/A
Study type: Interventional

The aim of this study is the first aim of a NIH project that consists of 3 aims. The first aim examines the acute effects of two high-quality milk proteins (casein vs. whey) on whole-body and muscle protein metabolism in COPD patients with severe loss of muscle mass and the effects of adding leucine. The principal endpoints will be the extent of stimulation of net whole body protein synthesis as this is the principal mechanism by which either amino acid or protein intake causes muscle anabolism. After determining the optimal nutritional formulation based on the first aim we will continue to work on the second and third aim where fish oil supplementation will be part of the nutritional intervention as well.

NCT ID: NCT01154127 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of NVA237 on Exercise Endurance in Patients With Chronic Obstructive Pulmonary Disease (COPD)

GLOW3
Start date: June 2010
Phase: Phase 3
Study type: Interventional

The ability for patients with COPD to exercise is limited due to the deterioration of their lung function. NVA237 is being developed to treat COPD. This study is designed to look at how well NVA237 improves the ability to exercise in patients with moderate to severe COPD.

NCT ID: NCT01153321 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Investigation of the Effect of Oral Treatment With 100 mg AZD2423 in Subjects With Mild Chronic Obstructive Pulmonary Disease (COPD)

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to find out if AZD2423 can reduce inflammation in the lungs of patients with mild COPD.

NCT ID: NCT01151618 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Evaluating Forced Oscillation Technique (FOT) in Abolishing Flow Limitation

Start date: June 2010
Phase: N/A
Study type: Interventional

To validate the capability of the Respironics Synchrony ventilator to properly detect Expiratory Flow Limitation (EFL) as compared to the gold standard method of detecting EFL via the Mead and Wittenberger technique.