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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT04963023 Completed - Asthma Clinical Trials

Biomarkers of Chronic Obstructive Pulmonary Disease

BIOBPCO
Start date: June 15, 2021
Phase:
Study type: Observational

There are few studies about immunological explorations in COPD. Because of the complications of lung biopsies, analyses are generally made on blood samples instead of lung tissue. No study tried to classify COPD vs Asthma vs ACOS. The investigators wondered if there were differences in biomarkers between these groups. The investigators decided to open a pilot-study among COPD patients followed in Amiens-University Hospital. Each patient will be examined and a blood-test will be performed.

NCT ID: NCT04955405 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The 7-Visit Transition of Care Hospital to Home Intervention: A Pilot Study

Start date: January 31, 2022
Phase: N/A
Study type: Interventional

New approaches to care transitions must deploy a longer-term and more intensive program that provide an array of services that address underlying social determinants of health (e.g. lack of adequate social support, lack of self-efficacy in managing symptoms and medications, impoverished living conditions, inability to connect with primary care and access. In addition, programs must be adaptable to meet the specific needs of individual patients. Our collaboration of health services researchers, quantitative scientists, and physicians propose to develop and implement a 90-day intensive and comprehensive intervention to support newly discharged patients with COPD and/or CHF. The proposed intervention will utilize a three-person team (registered nurse, clinical social worker, and a pharmacist) to provide an array of medical and social services specifically targeted to meet the needs of individual patients and their families. Aim: To determine using a randomized control trial, whether participation in an intensive series of 7 home-visits that provide tailored medical and social services among newly discharged low-income Medicare patients with COPD and/or CHF results in a) better patient-reported outcomes and b) a reduced likelihood of repeat hospital care (ED use or hospitalization) relative to a group of patients who receive usual discharge instructions.

NCT ID: NCT04953611 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Quantitative Study on HRCT Phenotype of COPD

Start date: July 1, 2013
Phase:
Study type: Observational

To explore the HRCT phenotype of the combined COPD assessment staging system

NCT ID: NCT04952883 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Hydrogen Sulfide and Pulmonary Vascular Remodeling on HRCT in Patients With COPD

Start date: December 1, 2016
Phase:
Study type: Observational

HRCT was used to evaluate pulmonary vascular remodeling in COPD. The role of H2S in pulmonary vascular remodeling in COPD was analyzed, in order to provide a basis for seeking new therapeutic targets.

NCT ID: NCT04952363 Completed - COPD Clinical Trials

Whole-body Vibration on Mucus Clearance, the Quality of Life, and Exercise Capacity for Patients With Chronic Obstructive Pulmonary Disease

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

Although whole body vibration (WBV) is mainly designed to promote neuromuscular function, however, because of its vibration characteristics, whether it can provide additional effects on the sputum clearance for chronic obstructive pulmonary (COPD) disease patients, thereby improving the quality of life, and exercise capacity is still unknown.

NCT ID: NCT04929990 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Effect of Respiratory Muscle Training for Patients With COPD and Mild Cognitive Impairment

Start date: August 7, 2018
Phase: N/A
Study type: Interventional

Patients with COPD and MCI received either inspiratory muscle training or inspiratory plus expiratory muscle training and compared the therapeutic effects

NCT ID: NCT04928417 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Exacerbations and Their Outcomes International (EXACOS International)

EXACOS-Intl
Start date: November 26, 2021
Phase:
Study type: Observational

Observational, cross-sectional study with retrospective data collection from medical records. During the cross-sectional study visit, data will be captured through the use of electronic Case Report Forms (eCRFs). As there will be only one study visit, no prospective data collection will take place, nor collection of data that are not part of the routine clinic visit. For understanding the burden of severe exacerbations of COPD and the association between frequency of severe exacerbations and clinical and health-care utilization outcomes in less well-resourced countries

NCT ID: NCT04926233 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Characteristics and Treatment Patterns of Patients With Chronic Obstructive Pulmonary Disease (COPD), Initiating Tio+Olo or Other Maintenance Therapies in the US and the UK: A Retrospective Claims Database Study

Start date: November 15, 2019
Phase:
Study type: Observational

The primary objectives of the study are to use US and UK data to describe the characteristics of Chronic Obstructive Pulmonary Disease (COPD) patients according to various demographic, lifestyle, clinical, and medication use.

NCT ID: NCT04923347 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Study to Evaluate the Safety and Efficacy of Fluticasone Furoate (FF)/Umeclidinium(UMEC)/Vilanterol (VI) in Participants With Chronic Obstructive Pulmonary Disease (COPD)

Start date: June 6, 2023
Phase: Phase 4
Study type: Interventional

This study will evaluate safety and efficacy of FF/UMEC/VI via ELLIPTA® inhaler. ELLIPTA is a registered trademark of GlaxoSmithKline group of companies.

NCT ID: NCT04919200 Completed - Clinical trials for Obstructive Lung Disease

Optimized Single-breath Helium Lung Volume in Obstructive Lung Disease

Start date: January 1, 2018
Phase:
Study type: Observational

Whole-body plethysmography (WBP) is the gold standard for measuring lung volume, but its clinical application is limited because it requires expensive equipment and is complicated to use. Studies have shown that the single-breath helium dilution (SBHD) method, which is commonly used in clinical practice, significantly underestimates lung volume in patients with obstructive lung disease (OLD). Therefore, by comparing the differences in lung volume measured by the SBHD method and WBP in patients with different severities of obstructive lung disease, we aim to establish a correction equation for the SBHD method to determine the total lung volume in obstructive lung disease patients.