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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT00940355 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Secondary Prevention of Problems in Health Status in Patients With Chronic Obstructive Pulmonary Disease (COPD)

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

The purpose of this study is to determine the effectiveness of an intervention conducted by a pulmonary nurse in patients with COPD. The hypothesis is that in a sample of COPD patients with clinically relevant problems in health status (physiological functioning, symptoms, functional impairment and quality of life), a motivational intervention conducted by a pulmonary nurse will lead to patient-tailored treatment and an improved health status.

NCT ID: NCT00939211 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Study Will Evaluate the Effect of AZD9164 in Patients With Chronic Obstructive Pulmonary Disease

LaCrossE
Start date: June 2009
Phase: Phase 2
Study type: Interventional

Chronic Obstructive Pulmonary Disease (COPD) is a chronic respiratory condition with deteriorating lung function over the years. Patients with COPD experience symptoms of shortness of breath, cough and sputum production. This study is to assess the treatment effects after inhalation of three different single doses of AZD9164 (100, 400 and 1200 mcg) and one single dose of tiotropium (18 mcg). One dose of placebo will be given as comparator. 25 patients are to participate in the study and all will be recruited in Sweden. Each patient will visit the study doctor 9 times during the study, whereof 5 visits will be overnight visits. All examinations, treatment and the follow-up is free of charge.

NCT ID: NCT00935181 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Respiratory Muscle Stretching in Chronic Obstructive Pulmonary Disease (COPD)

Start date: January 2006
Phase: Phase 4
Study type: Interventional

Objective: The investigators studied the effects of respiratory muscle stretching in an 8-week pulmonary rehabilitation program. Methods: This was a simple-blind parallel controlled trial, conducted an out-patient clinic. Twenty six patients with COPD (mean age 68 ± 6 y, percent of predicted FEV1 47 ± 16) were randomized to either respiratory muscle stretching group plus exercise training (RMS), and exercise training group (Sham), in an 8-week exercise program that had 3 sessions per week. The investigators measured inspiratory and expiratory muscle strength (by maximal inspiratory and expiratory pressure - PIM and PEM), exercise capacity (by 6-minute walk distance), dyspnea and quality of life.

NCT ID: NCT00934713 Completed - Clinical trials for Signs and Symptoms, Respiratory

The Effect of Montelukast Treatment in Wheezy Infants

Montelukast
Start date: September 2004
Phase: Phase 4
Study type: Interventional

The study is designed to evaluate the efficacy of montelukast on symptom-free days in unselected group of very young children with wheeze and recurrent asthma like symptoms. The secondary aim was to evaluate the effect of montelukast on lung function, airway responsiveness, airway inflammation and use of rescue medication.

NCT ID: NCT00932646 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Characterisation of 24-hour FEV1-time Profiles of Inhaled BI 1744 CL and Inhaled Foradil in Patients With Chronic Obstructive Pulmonary Disease

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The study is intended to characterize the lung function profile of BI1744 in COPD patients where patients will perform pulmonary function tests at regular intervals for 24 hours at the end of a 6 week treatment period. Each patient will receive all four treatments.

NCT ID: NCT00931385 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Characterization of 24 Hour Spirometry Profiles of Inhaled BI 1744 CL and Inhaled Foradil in Patients With Chronic Obstructive Pulmonary Disease

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The study is intended to characterize the lung function profile of BI1744 in COPD patients where patients will perform pulmonary function tests at regular intervals for 24 hours at the end of a 6 week treatment period. Each patient will receive all four treatments.

NCT ID: NCT00929734 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Effect of Rosuvastatin Therapy in Patients With Stable Chronic Obstructive Pulmonary Disease

RODEO
Start date: March 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate whether rosuvastatin improves measures of endothelial function, decreases measures of inflammation, and improves pulmonary function in patients with stable chronic obstructive pulmonary disease.

NCT ID: NCT00929110 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

1-year Study to Assess the Efficacy, Safety, and Tolerability of Glycopyrronium Bromide (NVA237) in Chronic Obstructive Pulmonary Disease (COPD)

GLOW2
Start date: June 2009
Phase: Phase 3
Study type: Interventional

This study was designed to investigate the 1 year efficacy and safety of the 50 µg once daily (od) dose of glycopyrronium bromide (NVA237) in patients with moderate to severe chronic obstructive pulmonary disease.

NCT ID: NCT00925171 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Maintenance Schedules Following Pulmonary Rehabilitation

Start date: June 2009
Phase: Phase 2
Study type: Interventional

Chronic obstructive pulmonary disease (COPD), a preventable and treatable condition, is a major healthcare problem with huge human and economic costs. It affects 3 million people, results in 1.4 million consultations, causes 30,000 deaths, and costs £800M per year in the UK. Considerable research expenditure is devoted to finding new and expensive interventions. However pulmonary rehabilitation (PR) is an available therapeutic option with good evidence of benefit for patients in terms of quality of life and daily functioning. The primary objective of the study is to evaluate the effectiveness and cost effectiveness of the addition of a maintenance programme following pulmonary rehabilitation in patients with COPD when compared to standard care. The secondary objective is to identify baseline characteristics that will predict improvement in pulmonary rehabilitation programmes and adherence to maintenance strategies. By measuring a series of demographic, clinical, physiological, psychological and biochemical parameters the researchers hope to be able to predict those patients who are likely to receive the greatest benefit from pulmonary rehabilitation. An additional objective will be to prepare a detailed maintenance programme manual. This will be available to other centres providing pulmonary rehabilitation at the conclusion of the study

NCT ID: NCT00922545 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Evaluation of a Combined Strategy Addressed to Practitioners and Chronic Obstructive Pulmonary Disease (COPD) Patients to Improve Clinical Control and Quality of Life

Start date: April 2004
Phase: N/A
Study type: Interventional

Main objective: Evaluate the effectiveness of a combined strategy addressed to health care workers and patients, in relation to improving clinical control and patient's quality of life.It includes a feed-back about the health status of the patients, an education plan addressed to practitioners based in a CPG and in health education