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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT01381367 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

PPSV23 Pneumococcal Vaccine in Chronic Obstructive Pulmonary Disease (COPD)

Start date: February 2009
Phase: Phase 4
Study type: Interventional

Streptococcus pneumoniae is the most common causes of community-acquired pneumonia and exacerbations in chronic obstructive pulmonary disease (COPD) patients, which are associated with morbidity, mortality, and higher health-care cost. In addition, recently high daily dose of inhaled corticosteroid (ICS) therapy became more evident to be beneficial in moderate-to-severe COPD patients, but excess risk of pneumonia shown in database analysis was worried about by primary physicians. The use of pneumococcal polysaccharide vaccination (PPSV23) has protective efficacy to eliminate infection of Streptococcus pneumoniae from previous studies. If the use of PPSV23 can reduce the incidence of pneumonia or exacerbations in COPD patients using high daily dose of ICS, the benefit of ICS can be preserved and risk of pneumonia can be reduced. However, there is only limited data supporting this hypothesis. In this study, the investigators will conduct a double-blinded, randomized controlled trial to evaluate the clinical efficacy of PPSV23 in severe COPD patients using high daily dose of ICS.

NCT ID: NCT01380652 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Vibration Training in Chronic Obstructive Pulmonary Disease (COPD)-Patients During a Three-week Rehabilitation

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

The aim of this study is to investigate the change of physical activity in COPD-patients performing a whole body vibration training additional to a standard three-week rehabilitation program in comparison to patients performing merely a standard rehabilitation program.

NCT ID: NCT01380639 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of Vibration Training on Exercise Capacity in COPD-patients

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

The aim of this study is to investigate the exercise capacity in COPD-patients performing a vibration training additional to a standard three-week rehabilitation program in comparison to patients performing merely a rehabilitation program.

NCT ID: NCT01380626 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of Exercise Training in Chronic Obstructive Pulmonary Disease Versus Alpha-1-Antitrypsin-deficiency-patients

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

Chronic Obstructive Pulmonary Disease (COPD)-patients (caused by smoking-level) and Alpha-1-Antitrypsin-deficiency patients showed different developments during rehabilitation in regard to improvement of 6-minute-walking distance. The aim of this study is to investigate differences between training adaptations in COPD-patients and Alpha-1-deficiency patients. Both groups take part in a standardized multimodal 3-week-rehabilitation with strength and endurance training. In addition to conventional diagnostic procedures, muscle biopsies from the M. vastus lateralis will be conducted before and after rehabilitation program followed by biochemical, histochemical and immunohistochemical analysis of the probes.

NCT ID: NCT01380470 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Prevalence of Undiagnosed Chronic Obstructive Pulmonary Disease Sufferers in the Region of Murcia

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

The purpose of this study is determine the prevalence of undiagnosed Chronic Obstructive Pulmonary Disease (COPD) in population served and with exposure to cigarettes in the Region of Murcia

NCT ID: NCT01380405 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Educational Intervention for Managing Inhalers in Chronic Obstructive Pulmonary Disease (COPD) Patients

Start date: May 2011
Phase: N/A
Study type: Interventional

Given the importance of the correct use of inhalers by patients with Chronic Obstructive Pulmonary Disease (COPD) for the appropriate treatment of the disease, the self-care programme which will be assessed will consist of an educational intervention on the correct use of inhalers. For this aim, we have designed this study to assess the influence of both individualized and collective self care programmes about the correct use of inhalers improves the functional state of patients with COPD compared to when there is no educational intervention.

NCT ID: NCT01378520 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Ketoconazole on Breathlessness

KetoRLB
Start date: June 2011
Phase: Phase 4
Study type: Interventional

Beta-endorphins, which are naturally occurring narcotic substances, have been shown to alter the perception of breathlessness. Oral ketoconazole, an antifungal antibiotic, increases blood levels of beta-endorphins. The study hypothesis is that oral ketoconazole will reduce ratings of breathlessness induced by resistive breathing loads.

NCT ID: NCT01378039 Completed - Asthma Clinical Trials

Pathogenetic Mechanisms of Chronic Obstructive Pulmonary Diseases

CAPTA
Start date: June 2004
Phase: N/A
Study type: Interventional

Asthma and chronic obstructive pulmonary disease(COPD) are common diseases, which tend to even increase in many countries. Both from a clinical and a pathophysiological point of view, this is an important issue. However, an understanding of the relationship between the complex array of cells and mediators involved in asthma and COPD is not yet fully dissected which makes difficult to find a specific and sensitive panel of biomarkers that can reflect intensity of these pathological processes and can help to predict the individual outcome.

NCT ID: NCT01377675 Completed - Clinical trials for Education of Primary Care Clinicians

Web-based, Interactive Professional Education for Chronic Obstructive Pulmonary Disease

WipeCOPD
Start date: April 2011
Phase: N/A
Study type: Observational

This study involves the development and evaluation of a web-based, interactive education program on chronic obstructive pulmonary disease (COPD) for primary care clinicians. The research questions that this proposal addresses include: 1. Can an interactive, web-based COPD course be developed to disseminate evidence-based, best practice recommendations to primary care clinicians? 2. Can assessment tools be developed to evaluate the impact of the program on clinician behavior in clinical practice and on patient care?

NCT ID: NCT01377428 Withdrawn - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Efficacy of Indacaterol 150 µg Versus Formoterol

Start date: September 2011
Phase: Phase 4
Study type: Interventional

The study will be a 12 week treatment (84 days), parallel group, randomized, double blind, double dummy, study to assess the superiority of indacaterol (150 μg o.d.) versus formoterol (12 μg b.i.d.) in terms of trough forced expiratory volume in 1 second (FEV1). Patients will be enrolled after giving informed consent and then begin a screening/run-in period for 14 days. Patients will be randomized to one of two treatment groups using an allocation ratio of 1:1 to receive either indacaterol (150 μg o.d.) and placebo to formoterol, or formoterol (12 μg b.i.d.) and placebo to indacaterol for a treatment period of 12 weeks.