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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: NCT00419744 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

A Comparison of SYMBICORT® pMDI With Formoterol Turbuhaler® in Subjects With COPD

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

The purpose of this study is to determine if SYMBICORT® delivered via a pressurized metered-dose inhaler, referred to as a pMDI, is effective in preventing COPD exacerbations.

NCT ID: NCT00419289 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Optimizing the Effect of COPD Rehabilitation

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

Patients with Chronic Obstructive Pulmonary Disease (COPD) may benefit from an 8-week pulmonary rehabilitation programme. However, the effect of the programme tends to attenuate with time. Patients who complete the programme are randomized to continued rehabilitation follow-up and control follow-up.

NCT ID: NCT00418613 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

A Research Study of MK0633 in Patients With Chronic Obstructive Pulmonary Disease (COPD)(0633-009)(COMPLETED)

Start date: January 2008
Phase: Phase 2
Study type: Interventional

A clinical study to evaluate the efficacy and safety of MK0633 in patients with Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT00417755 Not yet recruiting - COPD Clinical Trials

Effect of Invasive and Non Invasive Mechanical Ventilation on Feeding Delivery in COPD Elderly Patients

Start date: January 2007
Phase: Phase 4
Study type: Observational

COPD patients requiring ventilation may benefit from invasive or non invasive ventilation. Non invasive ventilation is often incompatible with oral or enteral feding, due to gastric dilatation and full mask therapy. At the other hand, invasive ventilation is associated with incomplete enteral feeding and nutrition requirements are not reached. The aim of the study was to compare the feeding delivery of COPD patients receiving invasive or non invasive mechanical ventilation.

NCT ID: NCT00415753 Completed - COPD Clinical Trials

Procalcitonin as a Marker of Bacterial Pneumonia

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

Objective: To evaluate PCT as a marker of bacterial community acquired pneumonia in a Danish Hospital setting. To test if it is possible to reduce the use of antibiotics and the length of stay in hospital, and the willingness of the clinicians to take this new marker under advisement in their choice of treatment. The study is a randomised, controlled intervention study. All adult patients admitted to the Department of Infectious Disease at Skejby hospital suspected of a lower respiratory tract infection (e.g. CAP, acute exacerbation of COPD and bronchitis) are eligible for inclusion. Patients are randomised to have either PCT guided treatment or standard care, in which case the doctor will not learn the PCT test result. In the PCT group the antibiotic treatment will be based on serum PCT as follows: If PCT is less than 0.25 µg/L antibiotic treatment is discouraged; if PCT is greater than 0.25 µg/L antibiotic treatment is encouraged and if PCT is greater than 0.5 µg/L antibiotic treatment is strongly encouraged. The treating doctor is allowed to overrule the treatment guidelines. The control group will receive antibiotics according to usual practice. The primary endpoints are antibiotic use and length of stay in hospital. Secondary endpoint is the proportion of patients where the treating doctor chooses to disregard the guidelines.

NCT ID: NCT00413543 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Pulmonary Rehabilitation for Chronic Obstructive Pulmonary Disease (COPD) Exacerbation

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

This is a study to evaluate the effects of early pulmonary rehabilitation within 10 days after discharge from the hospital after a COPD exacerbation on exercise tolerance, exacerbations, re-admissions and the quality of life during 6 months.

NCT ID: NCT00412204 Completed - COPD Clinical Trials

Study to Evaluate the Effects of Tiotropium Bromide on Chronic Obstructive Pulmonary Disease (COPD) During Exercise

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

The purpose of this study is to determine the effect of treatment with tiotropium bromide on efficiency of gas exchange and exercise performance in COPD subjects during exercise.

NCT ID: NCT00406705 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Effect of Breathing Helium-Hyperoxia During Pulmonary Rehabilitation in Patients With COPD

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

The purpose of this study is to examine whether breathing helium-hyperoxia during exercise in a pulmonary rehabilitation program can improve the exercise tolerance and health related quality of life of patients with Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT00405236 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Tiotropium on Inflammation and Exacerbations in COPD

Start date: October 2002
Phase: Phase 4
Study type: Interventional

Patients with COPD experience exacerbations that are a major cause of morbidity. Exacerbations are associated with increased airway and systemic inflammation and those experiencing frequent exacerbations demonstrate increased inflammation in the stable state. Tiotropium has been shown to reduce exacerbation frequency and it might be postulated that this is due to a reduction in inflammation. The study will compare airway inflammation and exacerbation frequency in patients with COPD on tiotropium or placebo.

NCT ID: NCT00404430 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Protocol Chronic Obstructive Pulmonary Disease

Start date: January 11, 2007
Phase:
Study type: Observational

The main objective of the study is to evaluate the predictive factors of the endothelial function to the waning of an acute exacerbation in COPD. It will act to do a multivariate analysis to determine the respective weight of the parameters of the systemic inflammation, of the oxidative stress of the functional respiratory parameters and then functional respiratory parameters. In exacerbated Chronic Obstructive Pulmonary Disease (COPD) patients, there is augmentation of hypoxia and the obstructive ventilatory disorders is more important. This is correlated with an increase in C-reactive Protein (CRP) and of inflammatory cytokines and oxidative stress. It has been demonstrated that there is an endothelial dysfunction in answer to hypoxia. Since the exacerbated COPD patients are hypoxic in most cases , we suppose they have an endothelial dysfunction during exacerbation. So we think we will find an augmentation of vascular resistances ,shown by a peripheral arterial tone too high. And this, certainly, play a part in physiopathology of the COPD exacerbation.