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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: NCT00546299 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Gas Usage for Those With COPD Who Experience Low Oxygen Levels During Activities Only

Start date: February 2003
Phase: N/A
Study type: Interventional

Several studies have described the use of supplemental oxygen during exertion or activities of daily living (ambulatory oxygen) in study populations that have different characteristics. This report, based on specialized randomized controlled trials, characterizes ambulatory gas usage among patients with COPD who experience low oxygen levels during activities.

NCT ID: NCT00545922 Completed - Depression Clinical Trials

Cognitive Behavioral Therapy for Anxiety and Depression in COPD

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

The purpose of this study was to examine the efficacy of manualized, short-term group cognitive behavioral therapy for COPD patients suffering from clinically significant symptoms of anxiety and/or depression.

NCT ID: NCT00545311 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Safety and Tolerability of Multiple Inhaled NVA237 Doses in Chronic Obstructive Pulmonary Disease (COPD) Patients

Start date: July 2007
Phase: Phase 1
Study type: Interventional

This study will evaluate the pharmacokinetics, pharmacodynamics and safety of multiple doses of the NVA237 in mild and moderate COPD patients .

NCT ID: NCT00542932 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

The Effects of a Home Exercise Video Programme for Patients With COPD

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

Patients with COPD, suffer symptoms of breathlessness and leg weakness. Exercise programmes in the form of pulmonary rehabilitation (PR) have been shown to improve both of these symptoms significantly. PR involves patients attending a hospital or community centre. For some patients, leaving the house is an ordeal. This study investigated the effectiveness of an exercise video programme delivered in the patients home.

NCT ID: NCT00542880 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Evaluation of Onset of Effect in Patients With Severe Chronic Obstructive Pulmonary Disease (COPD) Treated With Symbicort® Compared to Seretide®

SPEED
Start date: September 2007
Phase: Phase 4
Study type: Interventional

This study is to assess the effects with two different inhaled respiratory medications with regards to improvement of lung function, symptoms and morning activities.

NCT ID: NCT00542282 Completed - Asthma Clinical Trials

Vibration Response Imaging in Chronic Obstructive Pulmonary Disease and Asthma

Start date: November 2006
Phase: N/A
Study type: Observational

Obstructive lung disease is usually a differential diagnostic consideration when a patient presents with breathlessness or cough. Spirometry is the key diagnostic test used to confirm airflow obstruction particularly in the primary care setting. Airflow obstruction that completely resolves after administration of a bronchodilator, by definition, excludes a diagnosis of COPD. Evaluation of obstructive lung disease must include pulmonary function testing; bronchoreversibility testing is an adjunct in differentiating between asthma and COPD. Bronchoreversibility cannot serve as an absolute diagnostic criterion for separating asthma from COPD. Vibration response imaging (VRI) technology provides a simple, radiation-free method to image the lungs, by visualizing vibration energy (lung sounds) emitted during respiration cycle. In this study, regional quantitative and qualitative information on vibration response is compared with spirometry in assessing lungs function of COPD and Asthma patients.

NCT ID: NCT00540163 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Observational Non-interventional Study With Spiriva in Chronic Obstructive Pulmonary Disease Patients With Exercise-induced Dyspnoea

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

This observational non-interventional study is designed to demonstrate the improvement of physical function in COPD patients with exercise-induced dyspnoea on treatment with Spiriva (tiotropium 18 µg capsules) and allows adverse events to be recorded and evaluated.

NCT ID: NCT00532350 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Safety and Tolerability QAT370 Compared to Tiotropium in Patients With Chronic Obstructive Pulmonary Disease

Start date: July 2007
Phase: Phase 1
Study type: Interventional

This study will assess the safety and tolerability of QAT370 compared to tiotropium in patients with COPD.

NCT ID: NCT00531791 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Effects of Advair® in Outpatients With Chronic Obstructive Pulmonary Disease (COPD) Acute Exacerbation

Start date: November 2007
Phase: Phase 3
Study type: Interventional

Short course of steroids in COPD exacerbation improves FEV1 and decreases the relapse rate. However, some concerns remain about using systemic steroids for all patients with acute exacerbation. Their short-term advantages may be outweighed by the occurrence of adverse side effects such as hyperglycemia, which is difficult to manage on an outpatient basis. In this context, the possibility of treating patients with COPD exacerbation with inhaled steroids having less systemic adverse effects is interesting. The objectives are to compare relapse rate, lung function, the severity of dyspnea and, systemic and sputum inflammatory markers in outpatients with acute COPD exacerbations treated with fluticasone/salmeterol (Advair®) or oral prednisone for 10 days. The hypothesis is that Advair® is as effective as prednisone in treatment of outpatients with COPD exacerbation. The primary endpoint is to determine if the relapse rate at one month is equivalent for both treatments. The secondary endpoints are to compare lung function and dyspnea score and, systemic and sputum inflammatory markers modulation after 10 days of both treatments. We will recruit 30 outpatients in each group from our COPD clinic. Patients will receive prednisone (40mg/day) with placebo diskus or Advair® 50/500ug 2 inhalations bid (twice the regular dose) with placebo pills for 10 days. All patients will receive antibiotics and short-acting bronchodilators as needed. We expect to demonstrate that the improvement of lung function, dyspnea, inflammatory markers and relapse rate are equivalent in both treatments suggesting that Advair® could be a good alternative to prednisone for patients with steroid-induced hyperglycemia.

NCT ID: NCT00531050 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Safety of Exercise and High-dose Salbutamol in Patients With Chronic Obstructive Pulmonary Disease (COPD) Receiving Therapeutic Doses of Indacaterol (QAB 149) and Salmeterol

Start date: August 2007
Phase: Phase 2
Study type: Interventional

This study investigated the effect of exercise and high-dose salbutamol on the maximum heart rate in patients with chronic obstructive pulmonary disease (COPD) receiving therapeutic doses of indacaterol, salmeterol and placebo.