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Lung Diseases, Obstructive clinical trials

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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: NCT04950023 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Small Bioactive Molecules in Early COPD Diseases

Start date: May 11, 2021
Phase:
Study type: Observational [Patient Registry]

To study the predictors contribute to the progression of COPD by follow-up of patients with early COPD and analyze their changes in bioactive molecular, exhaled gas, CT image, lung function, patient's symptoms and life quality.

NCT ID: NCT04939454 Recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Involvement of Skeletal Muscle Fibrocytes in sarcOpenia in Patients With Chronic ObstRuctive Pulmonary Disease

MOTOR
Start date: November 29, 2022
Phase: N/A
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) is presently the third leading cause of death worldwide and is characterized by irreversible airflow limitation diagnosed by spirometry. COPD is currently considered as a systemic disease with predominantly respiratory involvement, associated with numerous comorbidities. Among these, muscle wasting, present in about one third of patients, is associated with a higher mortality (up to 10-fold, irrespective of the severity of the obstruction). Muscle wasting is classically characterized by a decrease in muscle strength and volume (sarcopenia), which can be defined by a decrease in the muscle mass measured by dual X-ray absorptiometry: Appendicular Skeletal Muscle Mass or ASM / height < 7.0 kg/m2 in men and 5.5 kg/m2 in women. However, sarcopenia is largely underestimated in current clinical practice. Moreover, there is no specific treatment: only exercise training as part of respiratory rehabilitation has shown some efficiency. The underlying pathophysiological mechanisms are indeed poorly characterized. Fibrocytes, cells derived from blood monocytes and able to migrate to different organs in order to play pro-fibrotic or pro-inflammatory roles, play a key role in bronchial obstruction. They are recruited in the blood of COPD patients during an acute exacerbation according to a CXCL12/CXCR4 chemotactic axis. Their role in COPD sarcopenia is currently unknown, but recent data show that they are involved in a mouse model of muscular dystrophy. The hypothesis is that fibrocytes are involved in COPD sarcopenia.

NCT ID: NCT04932811 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

The Lung Microbiome and Endobronchial Valve Treatment

Start date: June 16, 2021
Phase:
Study type: Observational

Lung emphysema is often associated with chronic obstructive pulmonary disease (COPD) and without any cure. Dyspnea is the main, debilitating symptom and is relieved by inhaled bronchodilators and rehabilitation. However, a substantial number of patients continue to suffer from dyspnea and among these, many patients have severely hyperinflated lungs due to predominant emphysema. For selected patients, lung transplantation or lung volume reduction by surgical removal (LVRS) of the most emphysematous parts of the lung can improve symptoms and survival. However, LVRS is related to complications and not all patients are suitable for surgery. An alternative to LVRS is bronchial lung volume reduction with endobronchial valves (EBV). One-way valves are inserted in the bronchial system using a bronchoscope and it has emerged as a valid treatment option with similar effects as LVRS with reduction of hyperinflation and increasing pulmonary function, quality of life, and exercise capacity. The normal lung is colonized with several types of bacteria, and together this is called the microbiome. Some bacteria are potentially beneficial, while others are potentially harmful. After the insertion EBV, some patients develop chronic infections. The hypothesis is that the microbiome can affect the risk of this chronic infection, and therefore the objective of this study is to access the microbiome during the insertion of the EBV, and afterwards observe which patients develop chronic infection and if these patients are harbouring specific types of bacteria.

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.