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Lung Diseases clinical trials

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NCT ID: NCT00660738 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Functional Tests in Individuals With Chronic Obstructive Pulmonary Disease (COPD)

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

Objectives: to evaluate and compare the responses to the various functional tests, and the concordance between the six-minute walk test in hallway (6MWT) and the of oval track (6MWToT), of treadmill (6MWTT), and of treadmill with inclination (6MWTTI), the six-minute step test (6MST) and the sit-to-stand test (STST), in patients with Chronic Obstructive Pulmonary Disease (COPD), and to correlate the responses with functional state and quality of life. Methods: Ten patients with COPD (71±8years, FEV1<80%predicted) were assessed using the functional tests. A dyspnea was assessed using the London Chest Activity of Daily Living and the Medical Research Council scales; and the quality of life was assessed using the St George's Respiratory Questionnaire (SGRQ).

NCT ID: NCT00659529 Completed - Cystic Fibrosis Clinical Trials

Safety and Efficacy of Sildenafil in Cystic Fibrosis (CF) Lung Disease

Start date: August 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether sildenafil can decrease inflammation in CF lung disease.

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: 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: 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.

NCT ID: NCT00637299 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Osteopathy in Chronic Obstructive Pulmonary Disease (COPD) Rehabilitation Trial

Start date: January 2008
Phase: Phase 0
Study type: Interventional

The purpose of this trial is to verify if an osteopathic treatment added to usual pulmonary rehabilitation trial is able to improve the walking ability of COPD patients and if there is any influence on lung functionality.