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Chronic Disease clinical trials

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NCT ID: NCT00975195 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Inhaled Corticosteroid Withdrawal in Patients With Chronic Obstructive Pulmonary Disease

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

This is a randomised study to be conducted in patients with severe to very severe Chronic Obstructive Pulmonary Disease (COPD) to establish whether there is a need for these patients to be continuously treated with an inhaled corticosteroid on top of two potent long-acting bronchodilators. The study also aims to identify the type of patients who are likely to benefit from inhaled corticosteroid maintenance therapy.

NCT ID: NCT00969605 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Adaptive Support Ventilation in the Weaning of COPD

Start date: April 2007
Phase: Phase 4
Study type: Interventional

Adaptive support ventilation (ASV) is a closed loop ventilation mode that can act both as pressure support (PSV) and pressure controlled (PCV) ventilation. Weaning with ASV shows promising results mainly in post-cardiac surgery patients. The aim of this randomized controlled study was to test the hypothesis that weaning with ASV could reduce the weaning duration in patients with chronic obstructive pulmonary disease (COPD) when compared with PSV.

NCT ID: NCT00964405 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Phase I Study of GSK233705 in Healthy Japanese Male Subjects

Start date: September 20, 2008
Phase: Phase 1
Study type: Interventional

This is a randomised, double blind, placebo-controlled, 2-parts study to investigate the safety, tolerability, and pharmacokinetics of single and repeat inhaled doses of GSK233705 from a novel dry powder device in healthy Japanese male subjects.

NCT ID: NCT00964249 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Phase I Study of GW642444M in Healthy Japanese Male Subjects

Start date: September 20, 2008
Phase: Phase 1
Study type: Interventional

This is a randomized, double blind, placebo controlled, parallel-group, 7 day repeat dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of inhaled dose of GW642444M from a novel dry powder device in healthy Japanese male subjects.

NCT ID: NCT00962468 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

European Quality of Care Pathways Study on Chronic Obstructive Pulmonary Disease (COPD)

EQCP-COPD
Start date: May 2009
Phase: N/A
Study type: Interventional

Care pathways, a complex intervention to (re)organise, standardize and evaluate care processes, are used worldwide and in different kinds of settings. Although their international use, the impact is unclear. The European Quality of Care Pathways Study is the first international cluster Randomized Controlled Trial on the effect of care pathways for COPD patients. The hypothesis is that teams who work with care pathways for COPD patients deliver care that is more compliant to evidence based key interventions, have better patient outcomes and higher scores on team indicators than teams who do not work with care pathways.

NCT ID: NCT00962455 Completed - Asthma Clinical Trials

Feedback Reports and e-Learning in Primary Care Spirometry

FRESCO
Start date: November 2007
Phase: Phase 4
Study type: Interventional

Spirometry is a biomedical test to measure lung function in subject who (may) have a chronic respiratory condition. Performing the test requires a certain level of training and experience from the health care professional who conducts the test, and sufficient cooperation of the patient. Although the test is widely used in primary care in many countries, the quality of the test performance seems limited and needs improvement in order to avoid false-positive and false-negative test interpretations. In this study, the researchers investigated whether a combination of e-learning and bimonthly written performance feedback to family practice nurses and assistance regarding their spirometry tests improves the rate of adequate tests.

NCT ID: NCT00961038 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Study to Evaluate the Safety and Pharmacokinetics of Inhaled Ciprofloxacin in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD)

Start date: August 2009
Phase: Phase 1
Study type: Interventional

Objectives of the study are to investigate the safety, tolerability and levels of ciprofloxacin in the lung after single and multiple inhalative administration to patients with moderate to severe COPD (stage II-III according to GOLD Criteria)

NCT ID: NCT00952861 Withdrawn - Clinical trials for Pulmonary Disease, Chronic Obstructive

Antibiotics in Chronic Obstructive Pulmonary Disease (COPD)

TAExaCOP
Start date: October 2009
Phase: Phase 4
Study type: Interventional

It is not clear whether antibiotic therapy is needed in patients with mild to moderate exacerbation of chronic obstructive lung disease. The aim of the study is to compare the effect of 1 day of treatment with 6 days of treatment in patients who are admitted to hospital and being clinical stable (as judged by their physician) 24 hours after hospitalization

NCT ID: NCT00950807 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

GSK573719 Dose Ranging Study in Chronic Obstructive Pulmonary Disease

Start date: September 1, 2009
Phase: Phase 2
Study type: Interventional

The study will evaluate the dose response, safety, and pharmacokinetics of GSK573719 compared with placebo in subjects with COPD.

NCT ID: NCT00939146 Completed - Heart Failure Clinical Trials

Outlook: An Intervention to Improve Quality of Life in Serious Illness

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

This study will demonstrate whether an end-of-life preparation and completion intervention reduces anxiety, depression, pain and other symptoms and improves functional status, spiritual well-being, and quality of life. If effective, the intervention offers a brief, inexpensive, and transportable non-physician treatment method for improving the experience of individuals in the latter stages of life-limiting illness.