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Lung Diseases clinical trials

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NCT ID: NCT00355342 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Bone Mineral Density Study In Patients With Chronic Obstructive Pulmonary Disease. DISKUS® Inhaler is a Trademark of the GSK Group of Companies.

Start date: April 28, 2004
Phase: Phase 4
Study type: Interventional

This study will last up to 3 years. You will visit the clinic up to 14 times. Certain visits will include lung function tests and scans of your bones. The purpose of this study is to determine the effect of the steroid component of an inhaled product on bone mineral density in patients with Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT00354666 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Single Doses GSK159797 On Patient Safety And Lung Function In Patients With Mild To Moderate Asthma

Start date: September 2004
Phase: Phase 2
Study type: Interventional

This study was designed to test safety aspects and effects on lung function of a new dry powder version of GSK159797 for asthmatic subjects to inhale. This will allow comparison with previous studies which have only used inhalation of the drug as a vapour.

NCT ID: NCT00354354 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Bronchodilators and Oxygen Kinetics With Exercise in Chronic Obstructive Pulmonary Disease (COPD) Patients

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

Hypothesis: The reduction of dynamic hyperinflation and its negative effects on the respiratory system following a bronchodilator could lead to an improvement of cardiac function in terms of increased cardiac output. This may enhance oxygen delivery to the exercising muscles in COPD patients. Bronchodilator administration may also have an indirect effect on V'O2 kinetics via its action on cardiovascular and pulmonary variables. Objectives: 1. To evaluate the effects of a bronchodilators on V'E , V'CO2 , and V'O2 kinetics in COPD during constant work-rate cycle exercise, and to evaluate whether bronchodilators will accelerate, indirectly, phase 2 kinetics (usually slower in COPD patients than normal subjects) and shorten t for V'E, V'CO2 , and V'O2 and shorten half-times for HR and O2 pulse, thus showing an improvement of oxygen transport to the peripheral active muscles. 2. To determine the impact of a bronchodilator-induced reduction in dynamic hyperinflation, and its effects on cardiovascular and pulmonary function, on exercise limitation in COPD.

NCT ID: NCT00347139 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Repeat Doses Of A New Medication (GW642444) In Asthmatic Patients

Start date: May 23, 2006
Phase: Phase 2
Study type: Interventional

In order to obtain information on a wider range of doses of GW642444 (a possible new medication to treat asthma) than has been previously examined in asthmatic patients, this current study will be conducted at doses of 25 100 and 400 mcg of GW642444 and will be compared with salmeterol (50 mcg twice daily). This study will be conducted in a similar manner to a study that has already been completed (study number B2C101762) which examined repeat doses of 50, 100 and 200 mcg of GW642444. The data obtained will compliment the data from study B2C101762 and will provide confidence (or not) that the desired bronchodilation can be achieved and maintained without undesirable side effects.

NCT ID: NCT00345774 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Safety and Effectiveness of PRX-08066 in Patients With Pulmonary Hypertension and Chronic Obstructive Pulmonary Disease

Start date: June 2006
Phase: Phase 2
Study type: Interventional

This study is being conducted to see if PRX-08066 can lower pulmonary artery pressures in patients with pulmonary hypertension associated with chronic obstructive pulmonary disease.

NCT ID: NCT00338507 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Phase 2 Study - Erdosteine in Patients With CB/COPD

Start date: March 2006
Phase: Phase 2
Study type: Interventional

This clinical study is designed to explore dose ranging and identify methods to demonstrate the efficacy of Erdosteine in patients with stable Chronic Bronchitis associated with Chronic Obstructive Pulmonary Disease.

NCT ID: NCT00328484 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Comparison of Two Programs to Encourage Physical Activity in Individuals With Chronic Obstructive Pulmonary Disease

Start date: January 2002
Phase: Phase 3
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) is a chronic lung disease. Symptoms include shortness of breath, wheezing, and difficulty exercising. Increasing exercise and physical activity may relieve the symptoms of COPD and may also slow the progression of the disease. The purpose of this study is to evaluate the effectiveness of a lifestyle activity program versus a traditional exercise program at increasing the amount of physical activity among individuals with COPD.

NCT ID: NCT00325897 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Macrolide Azithromycin to Prevent Rapid Worsening of Symptoms Associated With Chronic Obstructive Pulmonary Disease

Start date: March 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if long-term administration of a macrolide antibiotic will reduce worsening of symptoms among individuals with chronic obstructive pulmonary disease (COPD).

NCT ID: NCT00325169 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

SERETIDE Plus Tiotropium Versus Individual Components

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This study was designed to evaluate the effects on lung function of a combination of SERETIDE 50/500mcg twice daily plus tiotropium bromide 18mcg once daily compared with the individual treatments (tiotropium bromide 18mcg once daily alone and SERETIDE 50/500mcg twice daily alone) in subjects with COPD. The study will utilise a three-way cross-over design with a 2-week wash-out period between each 2-week consecutive treatment period.

NCT ID: NCT00322868 Completed - Cystic Fibrosis Clinical Trials

Safety and Efficacy of Pioglitazone as an Anti-inflammatory for the Treatment of Cystic Fibrosis (CF) Lung Disease

Start date: April 2006
Phase: N/A
Study type: Interventional

Study Hypothesis: Pioglitazone may decrease inflammation in cystic fibrosis lung disease. Primary outcomes: Markers of inflammation (neutrophils, elastase, cytokines and bacteria)will be measured in induced sputum specimens before and after a 4 week treatment period with pioglitazone in clinically stable CF patients.