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Chronic Obstructive Pulmonary Disease clinical trials

View clinical trials related to Chronic Obstructive Pulmonary Disease.

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NCT ID: NCT03871933 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Autonomic Function in COPD and Risk for Atrial Fibrillation

Start date: March 1, 2019
Phase:
Study type: Observational

In the presented study, autonomic function as well as risk for atrial fibrillation will be assessed to characterize the relation between risk of atrial fibrillation and autonomic function.

NCT ID: NCT03863821 Completed - COPD Clinical Trials

The Application and Analysis of HHHFNC in Walking Test of Pulmonary Rehabilitation

Start date: March 18, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the use heated humidified high-flow nasal cannula (HHHFNC) in pulmonary rehabilitation and analysis of cardiopulmonary parameters in adult patients.

NCT ID: NCT03859414 Completed - Asthma Clinical Trials

PK of BDP/FF/GB Single-inhaler Triple Therapy in Japanese vs. Caucasians

Start date: March 18, 2019
Phase: Phase 1
Study type: Interventional

The purpose of conducting this study is to obtain PK data of Beclometasone Dipropionate (BDP)/Beclometasone-17-MonoPropionate (B17MP), Formoterol Fumarate (FF) and Glycopyrronium Bromide (GB) after inhalation of CHF 5993 in Japanese as well as Caucasian healthy subjects under the same setting.

NCT ID: NCT03858348 Completed - COPD Clinical Trials

A Retrospective rEal-life daTa Study to Assess the exaceRbations and Lung functIon in Chronic Obstructive Pulmonary Disease ( COPD ) patiEnts receiVing Fluticasone/Salmeterol Comparing to Those Εscalating in Open-triple Fluticasone/Salmeterol, Long Acting Muscarinic Antagonist (LAMA) Combination

RETRIEVE
Start date: May 1, 2019
Phase:
Study type: Observational

Inhaled corticosteroid (ICS)/long-acting β2-agonist (LABA) combination is commonly prescribed to treat COPD; we will perform a retrospective analysis on the effect of adding a long-acting muscarinic receptor antagonist (LAMA) to ICS/LABA combination in COPD.

NCT ID: NCT03855670 Completed - COPD Clinical Trials

The Role of Physical Activity for Acute Exacerbations of COPD

Start date: November 29, 2018
Phase:
Study type: Observational

The investigators plan to study the association between physical activity, malnutrition and sarcopenia and the occurrence of acute exacerbations of COPD / the evolution of the COPD assessment test (CAT) over 1 year in a telehealthcare cohort of patients with COPD. The investigators hypothesize that malnutrition and/or sarcopenia at baseline and a decline in the fat-free mass index over time is associated with an increased rate of acute exacerbations of COPD and an increased CAT score meaning a higher risk for mortality, morbidity and impairment of quality of life.

NCT ID: NCT03853642 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Blood Eosinophil Measurements in Patients With Chronic Obstructive Pulmonary Disease

Start date: March 1, 2019
Phase:
Study type: Observational [Patient Registry]

This study will assess the within-day variation of blood eosinophils in patients with Chronic Obstructive Pulmonary disease (COPD) in stable state and determine if there is a correlation between the blood eosinophils and certain clinical parameters.

NCT ID: NCT03853174 Completed - COPD Clinical Trials

Exercise Training and Inflammatory Mediators in COPD

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) is widely spread all over the world. It is predicted to be the third leading cause of death by 2020[1]. COPD is a common, preventable treatable disease that is characterized by an airflow limitation which is not fully reversable[2].

NCT ID: NCT03848819 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Portable NIV on Operational Chest Wall Volumes in COPD

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The VitaBreath (Philips, Respironics) is a portable, handheld, battery powered, non-invasive ventilation device, that has been shown to reduce activity-related shortness of breath in patients with COPD. The VitaBreath device delivers 18 cmH2O inspiratory and 8 cmH2O expiratory pressures, but can only be used during recovery periods. A previous study (REC: 17/NE/0085) showed that use of the VitaBreath device during the recovery periods interspersing successive exercise bouts enhances exercise tolerance and reduces breathlessness compared to pursed lip breathing in patients with COPD. This was attributed to faster recovery from exercise-induced dynamic hyperinflation, assessed by volitional inspiratory capacity manoeuvres using a spirometer. However, inspiratory capacity manoeuvres are effort dependent, thus limiting the number of repetitions the patient can perform during exercise. In addition, investigation of the direct effect of the application of the VitaBreath device on dynamic hyperinflation was not possible due to the need to employ a spirometer for assessing inspiratory capacity. Optoelectronic plethysmography (OEP) allows continuous non-invasive assessment of end-inspiratory and end-expiratory volumes of the thoracoabdominal wall and its compartments, thereby facilitating assessment of dynamic hyperinflation on a breath-by-breath basis without the necessity to breathe via a spirometer. Unfortunately, OEP technology was not available at the time of our previous study. The investigators will use OEP to provide accurate breath-by-breath volume measurements during exercise and recovery to evaluate whether the VitaBreath device reduces total and compartmental thoracoabdominal wall volumes compared to the pursed lip breathing technique. Furthermore, the investigators will investigate the effect of use of the VitaBreath device on respiratory muscle activation and respiratory muscle oxygenation using OEP technology in conjunction with electromyography (EMG) and near inferred spectroscopy (NIRS), respectively to appreciate how the application of the VitaBreath device impacts on the operation and energy demands of the respiratory muscles as compared to control pursed lip breathing. The investigators hypothesised that the use of the VitaBreath device during the recovery periods interspersing successive exercise bouts will reduce the magnitude of dynamic hyperinflation in a greater extent compared to the pursed lip breathing technique.

NCT ID: NCT03842904 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

A Study Comparing the Effects of Trimbow to Fostair in COPD

TRIFLOW
Start date: December 13, 2018
Phase: Phase 4
Study type: Interventional

A randomised, open label 2-way cross-over study to compare the effects of inhaled Beclometasone/Formoterol/Glycopyrronium (TRIMBOW) pMDI to Beclometasone/Formoterol (FOSTAIR) pMDI on hyperinflation and expiratory flow limitation in moderate to severe chronic obstructive pulmonary disease (COPD).

NCT ID: NCT03840941 Completed - COPD Clinical Trials

The Effect of Frailty on Balance, Activities of Daily, and Exercise Capacity in COPD

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

The investigators aim to demonstrate whether balance, cognition and activities of daily living have changed in COPD patients with and without frailty.