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Lung Diseases clinical trials

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NCT ID: NCT00658853 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effective High Aerobic Intensity Endurance Training Regimes in Chronic Obstructive Pulmonary Disease (COPD) Patients

Start date: January 2004
Phase: N/A
Study type: Interventional

4 times 4 minutes interval training with and without hyperoxia is more effective than low intensity endurance training.

NCT ID: NCT00657293 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Arm Training in Patients With Chronic Obstructive Pulmonary Disease

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

Patients with chronic lung disease often report shortness of breath when they use their arms for simple activities of daily living such as dressing, lifting, shaving, bathing and brushing their hair and teeth. The best type of arm training for these patients is still unknown. The objectives of this study are to: - develop a feasible and safe arm training program (ATP) for these patients; - examine the effects of this ATP on quality of life, arm function, arm exercise capacity and symptoms during activities of daily living; - examine the effects of ATP on breathing responses during arm exercises.

NCT ID: NCT00655954 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Osteoprotegerin (OPG) in Induced Chronic Obstructive Pulmonary Disease (COPD) Sputum

Start date: January 2008
Phase:
Study type: Observational

Evaluation of OPG level as disease markers has also been reported. It has been showed that patients with coronary artery disease had higher serum OPG levels than healthy volunteers. Moreover, serum OPG levels correlate with the number of stenotic coronary arteries

NCT ID: NCT00655694 Withdrawn - Clinical trials for Pulmonary Disease, Chronic Obstructive

Genomic/ Proteomic/ Metabonomic Profiling in Chronic Obstructive Pulmonary Disease (COPD)

Start date: January 2005
Phase:
Study type: Observational

Chronic obstructive pulmonary disease (COPD) is a chronic disease characterized by progressive airflow obstruction, chronic cough and dyspnoea in advanced stages. We hope to develop a better understanding of lung disease. Information from these studies will only be used for research purposes, to help develop safer and more effective treatments for asthma and COPD.

NCT ID: NCT00652964 Recruiting - Clinical trials for Central Alveolar Hypoventilation Syndrome

PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood

Start date: September 2009
Phase: N/A
Study type: Observational

Detect the PHOX2B Mutation-confirmed congenital central hypoventilation syndrome

NCT ID: NCT00648245 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effectiveness and Safety of BIO-11006 Inhalation Solution to Treat the Overproduction of Mucus and Inflammation in COPD

BREATH-1
Start date: June 2008
Phase: Phase 2
Study type: Interventional

The symptoms associated with COPD include overproduction of mucus and inflammation in the lungs. Overproduction of mucus results in impaired lung function and it encourages bacterial growth and associated COPD exacerbations. Therefore, a treatment that inhibits mucus overproduction or blocks inflammation could benefit COPD patients. The drug under evaluation in this study, BIO-11006 Inhalation Solution, is a new drug that may inhibit overproduction of mucus and may have important anti-inflammatory properties.

NCT ID: NCT00642616 Terminated - Asthma Clinical Trials

Evaluate Safety of Technosphere® Insulin (TI) in Diabetic Subjects With Moderate Obstructive Pulmonary Disease

Start date: March 2009
Phase: Phase 3
Study type: Interventional

Examine the effects of TI in combination with an anti-diabetic regimen including inhaled insulin versus anti-diabetic treatment without inhaled insulin on lung function & pulmonary safety

NCT ID: NCT00642148 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A 12 Week Study To Assess Efficacy And Safety Of GW856553 In Subjects With Chronic Obstructive Pulmonary Disease (COPD)

Start date: February 14, 2008
Phase: Phase 2
Study type: Interventional

Phase IIa, randomised, double-blind, double-dummy, parallel group, multi-centre study in subjects diagnosed with moderate chronic obstructive pulmonary disease (COPD). The primary objective is to evaluate the effects of 12-weeks of treatment with GW856553 7.5 mg twice daily (BID) compared with placebo on the percentage of sputum neutrophils at 12 weeks. Twelve weeks of treatment with SERETIDE 50/500 BID will be compared with placebo for effect on sputum neutrophils as a positive control arm in the study

NCT ID: NCT00640315 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Single Dose Study in Patients With Chronic Obstructive Pulmonary Disease (COPD) Associated Pulmonary Hypertension.

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

This study is to demonstrate the safety, tolerability, pharmakokinetic and pharmacodynamic effect of a single oral dose of BAY63-2521 in patients with pulmonary hypertension due to chronic obstructive pulmonary disease (COPD).

NCT ID: NCT00639236 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effectiveness and Safety of Inhaling Hypertonic Saline in Patients With Chronic Obstructive Pulmonary Disease

Start date: May 2004
Phase: Phase 4
Study type: Interventional

The use of inhaled hypertonic saline has been extensively documented in asthma, bronchiectasis, cystic fibrosis and COPD as method of bronchial challenge and sputum induction, but studies that evaluated others endpoints are required. The objective of this study was to analyse the effects of inhaling hypertonic saline compared with placebo with respect to functional exercise capacity, dyspnoea and quality of life. In a double-blind randomised parallel placebo-controlled trial, conducted at the Clínicas Integradas of the Evangelical Faculty of Paraná,sixty-eight patients (age 67 ± 6.5 years; FEV1 38.9 ± 16.2 predicted) were randomised to inhale 3% hypertonic saline (n=34) or placebo (n=34), combined with a program of exercise, three times a week, for 8-weeks.