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Lung Diseases clinical trials

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NCT ID: NCT01944033 Completed - Clinical trials for Acute Exacerbation of Chronic Obstructive Airways Disease

β2-agonist Versus Ipratropium Bromide Associated With β2-agonists in Chronic Obstructive Pulmonary Disease Exacerbation

Start date: July 2013
Phase: Phase 3
Study type: Interventional

The effectiveness of β2-agonists in the treatment of exacerbations of COPD is already established. The purpose of this study is to compare the effectiveness of the β2-agonists alone in nebulization with the association β2-agonists + Ipratropium bromide in the treatment of an acute exacerbation of COPD consulting the emergency departement based on the clinical and arterial blood gas.

NCT ID: NCT01943552 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Ipratropium Bromide in Peri-Operative COPD

Start date: October 2013
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, parallel-group, multi-centre trial.The trial aims to evaluate efficacy of nebulized ipratropium bromide in Chinese peri-operative patients with COPD under general anaesthesia.

NCT ID: NCT01942889 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Antioxidants and Pulmonary Rehabilitation in COPD Patients

AREB-1
Start date: April 2012
Phase: N/A
Study type: Interventional

On the basis of published data and investigators results indicating that systemic redox in balance may contribute to the peripheral muscle dysfunction in COPD patients, the investigators propose a study testing the effects of antioxidants and exercise training in COPD patients. The results may have major implication in the improvement of pulmonary rehabilitation benefits

NCT ID: NCT01942499 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Community-Based Maintenance Exercise Program for COPD

Start date: November 2012
Phase: N/A
Study type: Interventional

It is well established that individuals living with chronic obstructive pulmonary disease (COPD) demonstrate significant improvements following a formal rehabilitation program. The problem lies in the fact that these functional improvements diminish over a 12 month period. This decline in function is associated with decreased participation, a decline in health status, and an increased need to access the healthcare system. The objective of this project is to evaluate the effectiveness of a post-rehabilitation community-based exercise program for individuals with COPD and compare the outcomes with those achieved through standard care. Individuals with COPD who have completed a previous rehabilitation program will be enrolled in the study. Study participants will be assigned randomly to either a year-long community exercise program or usual care. Those assigned to the community program will exercise twice weekly at a local community centre supervised by trained fitness instructors. A case manager will facilitate the transition from the hospital rehabilitation program to the community centre. The case manager will also be available to participants and instructors for consult as needed. Continuing to build on an established partnership with the City of Toronto, the case manager will ensure fitness instructors receive specialized training in order to properly supervise and support the individuals with COPD. Participants assigned to usual care group will receive standard care by their family physician and respiratory specialist. Functional status will be evaluated before the program begins and again at 6-months and 1-year. The outcome of each group will be compared to determine the effectiveness of the community exercise program. It is hypothesized that individuals who participate in the community exercise program will have better function and quality of life versus those individuals who receive standard care.

NCT ID: NCT01941225 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Inhaled Iloprost, Dynamic Hyperinflation, and Oxidative Stress in COPD Patients

Start date: September 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the role of the pulmonary vasculature in the development and progression of chronic obstructive pulmonary disease (COPD). To accomplish this, an inhaled prostacyclin (iloprost) will be given to patients with COPD and changes in oxidative stress and lung volumes during exercise will be measured.

NCT ID: NCT01937390 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Observational Study of Adherence to LABA / LAMA in Chronic Obstructive Pulmonary Disease (COPD)

Start date: November 6, 2011
Phase:
Study type: Observational

The objective of the study is to observe the effect of adherence to once-daily administered long-acting bronchodilators (long-acting ß2-agonists [LABAs] / long-acting muscarinic antagonists [LAMAs]) on patients health related quality of life (HR-QoL) and to assess the relation between symptoms improvement and adherence to Chronic Obstructive Pulmonary Disease (COPD) maintenance therapy

NCT ID: NCT01933984 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Individualized Dosing Schedule of Inhaled Bronchodilator for Endotracheally Intubated COPD Patients

Start date: August 2013
Phase: N/A
Study type: Interventional

This study evaluates whether individualized dosing schedule of inhaled bronchodilator is more effective than fixed dosing in reducing airway resistance of intubated COPD patients.

NCT ID: NCT01933789 Completed - Heart Failure Clinical Trials

Improving Communication About Serious Illness

ICSI
Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to improve care delivered to patients with serious illness by enhancing communication among patients, families, and clinicians in the outpatient setting. We are testing a new way to help patients share their preferences for talking about end-of-life care with their clinicians and families. To do this we created a simple, short feedback form. The form is designed to help clinicians understand what patients would like to talk about. The goal of this research study is to show that using a feedback form is possible and can be helpful for patients and their families.

NCT ID: NCT01933334 Completed - Systemic Sclerosis Clinical Trials

Safety and Tolerability of Pirfenidone in Patients With Systemic Sclerosis−Related Interstitial Lung Disease (SSc-ILD) (LOTUSS)

Start date: September 2013
Phase: Phase 2
Study type: Interventional

PSSc-001 (LOTUSS) This study is a Phase 2, multinational, open-label, randomized, parallel-group, safety and tolerability study of pirfenidone in patients with systemic sclerosis−related interstitial lung disease (SSc-ILD).

NCT ID: NCT01931644 Completed - Breast Cancer Clinical Trials

At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions

Start date: July 2013
Phase:
Study type: Observational

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