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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT02585752 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

A Study of Expiratory Pressure Modulation in Moderate to Severe COPD Patients - Phase 1b

ComfortCOPD
Start date: October 1, 2015
Phase: N/A
Study type: Interventional

Dynamic pulmonary hyperinflation (DH) and intrinsic positive end-expiratory pressure (PEEP) are well known problems in COPD patients with acute and chronic respiratory failure. Measurement of intrinsic PEEP level during both, invasive and non-invasive ventilation is of major importance since in some circumstances (e.g. during exercise or during exacerbations) it can significantly increase respiratory workload of COPD patients. Extrinsic PEEP applied during both, invasive and noninvasive ventilation is used to overcome intrinsic PEEP and therefore to avoid or reduce dynamic hyperinflation.

NCT ID: NCT02579850 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

2-arm Parallel Group Study of Fixed Combination of CHF 5993 vs Ultibro® in COPD Patients

TRIBUTE
Start date: May 29, 2015
Phase: Phase 3
Study type: Interventional

The aim of the present study is to evaluate the superiority of the fixed triple therapy with BDP/FF/GB at a daily dose of 400/24/50 mcg respectively with that of Ultibro® Breezhaler® (DPI), fixed combination of indacaterol 85 mcg and of glycopyrronium 43 mcg in COPD patients.

NCT ID: NCT02571582 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease and Allied Conditions

Predictors of Mortality in Patients With Advanced Lung Disease in Home Oxygen Therapy

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

Advanced Pulmonary Disease (PAD) is a condition that affects countless individuals around the world. Patients are often functionally very limited, with premature death, which is due to the disease itself or its complications. Currently, there are numerous monitoring centers of these patients to increase survival, reduce costs and humanize care in these patients.

NCT ID: NCT02566343 Completed - Clinical trials for Postoperative Complications

Preoperative Diagnostic Tests for Pulmonary Risk Assessment in COPD

PredicT
Start date: November 2014
Phase:
Study type: Observational

This prospective study intends to investigate the incidence of postoperative pulmonary complications (PPC) or in-hospital mortality in patients with COPD or at risk for COPD undergoing high-risk noncardiac major surgery and to identify relevant risk factors. This study aims to quantify and compare the diagnostic performance of preoperative functional tests, exercise capacity, clinical assessment tests and predictive scoring systems to predict PPC or in-hospital mortality in these patients.

NCT ID: NCT02563314 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease With Acute Exacerbation, Unspecified

Comparison of Two Oxygen Setting During Non-invasive Mechanical Ventilation of Chronic Obstructive Pulmonary Disease

OXYSET
Start date: March 22, 2017
Phase: N/A
Study type: Interventional

Hypoxaemic patients with exacerbations of chronic obstructive pulmonary disease (COPD) are at some risk of carbon dioxide (CO2) retention during oxygen therapy. Main mechanism of CO2 retention is believed to be reversal of preexisting regional hypoxic pulmonary vasoconstriction, resulting in a greater dead space. Risk of CO2 retention during mechanical ventilation remains controversial. Thus recent study suggested limited risk of CO2 retention with controlled oxygen supplementation during mechanical ventilation. Conversely, controlled oxygen supplementation might decrease dyspnea and respiratory workload, increase comfort and improve both urinary output and renal function.

NCT ID: NCT02563184 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Seasonal Influenza Vaccine, Quadrivalent Versus Trivalent in Patients With Advanced Chronic Obstructive Pulmonary Disease

Start date: September 2015
Phase: Phase 4
Study type: Interventional

To evaluate the magnitude of the humoral immune responses to quadrivalent vs trivalent influenza vaccines in adults between the age of 50 and 64 years with a prior diagnosis of GOLD Stage C and D COPD vs. those patients without COPD.

NCT ID: NCT02557958 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study

Start date: January 2009
Phase: Early Phase 1
Study type: Interventional

Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study.

NCT ID: NCT02557178 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Home-Based Health Management of COPD Patients

Start date: September 2016
Phase: N/A
Study type: Interventional

Minnesota HealthSolutions Corporation (MHS) proposes to develop and evaluate a program to motivate and monitor people with chronic obstructive pulmonary disease (COPD) to complete home exercise as part of pulmonary rehabilitation (PR). The proposed system has two components: home-based activity monitoring and health coaching. The investigators will conduct a randomized, wait-list controlled clinical study to evaluate the effects of the activity monitoring system and health coaching on quality of life and daily steps.

NCT ID: NCT02553096 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Exacerbation Self-management in COPD: The ACCESS Study

ACCESS
Start date: June 2015
Phase: N/A
Study type: Interventional

Aim is to test the effect of ACCESS ("Adaptive Computerized COPD Exacerbation Self-management Support"), a software application designed to support patients with COPD in self-management of exacerbations.

NCT ID: NCT02552732 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease

Nasal High Flow Therapy 30 Day Readmission Study

N3ADS
Start date: November 2015
Phase: N/A
Study type: Interventional

The aim of this feasibility study is to provide data for a subsequent randomized controlled trial to investigate if patient outcomes will be improved after an acute COPD exacerbation using domiciliary nasal high flow therapy (NHF) compared to standard care. This feasibility study will investigate the following: process, resources, management and scientific aspects of delivering NHF as an adjunct therapy in COPD patients.