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Lung Diseases clinical trials

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NCT ID: NCT01291303 Completed - Clinical trials for Acute Exacerbation of Chronic Obstructive Airways Disease

Optimization of Ventilator Setting for Acute Exacerbations of Chronic Obstructive Pulmonary Disease

NIMV01AECB
Start date: October 2009
Phase: N/A
Study type: Interventional

The analysis of flow and pressure curves generated by ventilators can be useful in the individuation of patient-ventilator asynchrony, notably in COPD patients. To date, however, a real clinical benefit of this approach to optimize ventilator setting has not been proven. The aim of the present study was to compare: optimized ventilation, driven by the analysis of flow and pressure curves, and standard setting (same initial setting, same time at the bedside, same physician, while the ventilator screen was obscured with numerical data always available). The primary aim was the normalization of pH at two hours, whilst secondary aims were change in PaCO2, respiratory rate, patient's tolerance to ventilation (all parameter evaluated at baseline, 30, 120, 360 minutes and 24 hours after the beginning of ventilation). 70 patients (26 females, aged 78±9 years, PaCO2 74±15 mmHg, pH 7.28±0.05, mean±SD) have been enrolled, with no basal difference between the two groups.

NCT ID: NCT01289327 Completed - Lung Disease Clinical Trials

Propofol Versus Midazolam+Alfentanil for Sedation During Bronchoscopy: Comparison by Cutaneous Carbon Dioxide Tension

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

Although propofol is a popular agent for sedation during flexible bronchoscopy, some clinicians have raised concerns that it may cause greater respiratory drive reduction than more common drugs. However, this factor is difficult to accurately examine with pulse oximetry. The introduction of a novel device that noninvasively measures carbon dioxide (CO2) levels can help to resolve this controversy. The aim of this study is to evaluate the safety of conscious sedation with midazolam+alfentanil compared to propofol.

NCT ID: NCT01287325 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Efficacy of DNK333 in Patients With COPD and Cough

Start date: September 2003
Phase: Phase 1/Phase 2
Study type: Interventional

This study evaluates the efficacy and safety of two weeks treatment of DNK333 in patients with COPD and cough.

NCT ID: NCT01286831 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Single Dose Study to Determine the Excretion, Balance and Metabolic Disposition of Radiolabelled GW642444.

Start date: May 18, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to characterise the metabolic disposition of radiolabelled GW642444 when administered orally.

NCT ID: NCT01285492 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Long Term Safety and Tolerability of QVA149 Versus Tiotropium in Japanese Patients With Chronic Obstructive Pulmonary Disease (COPD)

Start date: January 2011
Phase: Phase 3
Study type: Interventional

This is a 52-week treatment, multi-center, randomized, open label, parallel group study to assess the long term safety and tolerability of once-daily QVA149 (indacaterol and NVA237 ([glycopyrronium bromide]) using tiotropium as an active control in Japanese patients with moderate to severe chronic obstructive pulmonary disease (COPD).

NCT ID: NCT01285167 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Quality of Life in Daxas-treated Patients Older Than 18 Years With Severe Chronic Obstructive Pulmonary Disease (COPD) (DACOTA)

DACOTA
Start date: August 2010
Phase: N/A
Study type: Observational

Chronic obstructive pulmonary disease (COPD) is a progressive and largely irreversible lung disease characterized by chronic bronchitis and/or emphysema, resulting in breathlessness, cough and sputum. As COPD progresses, patients experience increasing deterioration of their health-related quality of life, with greater impairment in their ability to work and declining participation in social and physical activities. The aim of this non-interventional study is to evaluate data on quality of life in COPD patients in Germany in a real life medical setting under therapy with the phosphodiesterase-inhibitor (PDE-4) roflumilast (Daxas). Evaluation is based on two COPD specific questionnaires to assess the patient`s health status over six months. During the study, lung function measurements such as spirometry will be conducted according to common medical standard. Daxas (tablet) will be administered once daily. The study will provide further data on the safety and tolerability of Daxas.

NCT ID: NCT01283984 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

AZD2115 Single Ascending Dose Study

Start date: January 2011
Phase: Phase 1
Study type: Interventional

AZD2115 Single Ascending Dose Study

NCT ID: NCT01283685 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Breathing Helium-Hyperoxia During Exercise in Patients With Chronic Obstructive Pulmonary Disease

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

Regular exercise can help patients with the lung disease, chronic obstructive pulmonary disease (COPD). But COPD patients have a hard time with training because of their breathing. To improve their program they can train with one leg at a time. Another way is to make their exercise easier by breathing helium. Putting two methods, one-legged and helium, together may improve their program even more. This project is planned to assess whether breathing helium improves their one-legged exercise endurance. If it does, then there may be a reason for combining one-legged exercise with breathing helium as part of their respiratory rehabilitation program. The aim of this study is to determine whether breathing helium-hyperoxia enables a further increase in the constant power endurance time during one-legged exercise in ventilatory limited subjects with COPD. The null hypothesis is that patients will have sufficient peripheral muscle limitation that ventilatory unloading using helium-hyperoxia will be of no additional benefit to exercise tolerance. The investigators hypothesize that patients with COPD are so ventilatory limited relative to their peripheral muscles that helium-hyperoxia will improve their exercise endurance.

NCT ID: NCT01274507 Completed - Asthma Clinical Trials

A Study for Disease Profiling of Asthma and Chronic Obstructive Pulmonary Disease

Start date: July 2010
Phase: Phase 0
Study type: Interventional

The purpose of this study is to characterize the clinical, physiologic, and molecular profiles of healthy participants, participants with mild, moderate, and severe asthma; and participants with moderate to severe Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT01273298 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of Cardioselective β-blockers on Dynamic Hyperinflation in COPD

Start date: June 2008
Phase: N/A
Study type: Interventional

Patients with chronic obstructive pulmonary disease (COPD) are at greater risk of suffering from diseases for which beta-blockers may be indicated and effective. Clinicians remain hesitant to administer beta-blockers to COPD patients for fear of adverse effects on lung function. However, cardioselective beta-blockers therapy led to a non-significant worsening of resting expiratory flow limitation measured by the forced expiratory volume in one second (FEV1) as compared to placebo. But, the FEV1 appears to be a crude estimate bronchial obstruction in COPD. Importantly, the effects of cardioselective beta-blockers on dynamic hyperinflation, a subtle marker of bronchial obstruction, remain unknown. Thus, a prospective placebo-controlled study assessing the effects of short-term cardioselective beta-blocker therapy on dynamic hyperinflation in patients with moderate-to-severe COPD is needed.