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Lung Diseases, Obstructive clinical trials

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NCT ID: NCT02634983 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

QVA Mechanistic Efficacy Study (Receptor Effects, Etc)

Start date: June 3, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study was to assess global ventilated lung volume in moderate to severe COPD patients using MRI lung imaging after treatment with QVA149 compared to placebo.

NCT ID: NCT02631434 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Comparison Between Sit-to-stand Test and Six-minute Walk Test in Chronic Obstructive Pulmonary Disease

Start date: August 2013
Phase: N/A
Study type: Interventional

Comparison between sit-to-stand test and six minutes walking test in chronic obstructive pulmonary disease patients

NCT ID: NCT02629432 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Image-Based Structural and Functional Phenotyping of the COSYCONET Cohort Using MRI and CT

MR-COPD
Start date: December 2013
Phase: N/A
Study type: Observational [Patient Registry]

The main objective of this trial is to prove that MRI - as the imaging modality without the use of ionizing radiation - can replace CT for structural and functional regional phenotyping of COPD. The identification of different COPD phenotypes, such as the "emphysema-type" and the "airway-type", is important because therapy and prognosis will be different. The medical problem addressed in this trial is the image-based phenotyping of COPD. The sensitivity and specificity of MRI will be compared to Lowdose-CT serving as the gold standard. MRI and CT of the lung will be performed in a multi-centre cohort of 625 COPD-patients from the main COSYCONET cohort. The reliability of the MRI results will be demonstrated. MRI phenotypes will be evaluated visually and using software with quantitative read-outs. The agreement of both will be determined. The additional information of MRI over CT will be assessed.

NCT ID: NCT02629055 Terminated - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Respiratory EMG for NIV Titration in Stable COPD Patients

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

The aim of the present study is to investigate whether additional titration on surface electromyography (EMG) of the diaphragm and intercostal muscles improves the outcome of chronic non-invasive ventilation in patients with COPD and stable chronic hypercapnic respiratory failure in terms of better gas exchange after six weeks, lung function, patient comfort and compliance, and less patient ventilator asynchrony. Therefore, the investigators set up a randomized, two-armed crossover trial comparing regular titration with additional respiratory EMG titration of NIV.

NCT ID: NCT02628769 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Study to Evaluate the Anti-inflammatory Effects of Solithromycin in Chronic Obstructive Pulmonary Disease

Start date: July 2015
Phase: Phase 2
Study type: Interventional

This study examines the potential benefit of a new antibiotic, Solithromycin, for the long-term treatment of Chronic Obstructive Pulmonary Disease (COPD). Solithromycin is hypothesised to work by reducing inflammation in the lungs of patients with COPD. Stable COPD patients will receive treatment with solithromycin for 28 days and comparisons will be made between any effects observed with Solithromycin and a placebo. This will include any changes in inflammatory proteins, lung function and reported symptoms.

NCT ID: NCT02627872 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Clinical & Systems Medicine Investigations of Smoking-related Chronic Obstructive Pulmonary Disease

COSMIC
Start date: March 2007
Phase:
Study type: Observational

Chronic Obstructive Pulmonary Disease (COPD) is an increasing global health problem, which primarily increases among the female population. The purpose of this study is to perform in-depth clinical and molecular characterizations of early stage COPD patients, as well as healthy never-smoker and at-risk smoking control populations to identify molecularly related subgroups patients, including gender-related sub-phenotypes of COPD.

NCT ID: NCT02626468 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Validation of Structured Light Plethysmography - Health and Disease

SLP-RespDis
Start date: March 2013
Phase:
Study type: Observational

Validation of Structured Light Plethysmography (SLP) in patients with conditions such as Chronic Obstructive Pulmonary Disease (COPD) that effect breathing and in healthy participants.

NCT ID: NCT02618746 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Home Rehabilitation Via Telemonitoring in Patients With COPD

TELECARE
Start date: December 2013
Phase: N/A
Study type: Interventional

COPD is the fourth leading cause of death in the world and is the only one of the top five illnesses whose death rate is still increasing. It is mainly caused by smoking. Greece has a higher prevalence and death rate for COPD than many other countries in Europe. The disease is incurable so treatment is aimed at alleviating symptoms and slowing progression. Despite maximal medication and strategies such as pulmonary rehabilitation and home nurse support, many patients remain vulnerable, socially isolated and report difficulty in accessing their local health services. Research has shown that patients have worsening symptoms for an average of three to four days before they are admitted to hospital with an exacerbation of COPD. This suggests a window of opportunity to intervene. Early warning and contact via innovative technology may treat symptoms earlier, improve patient confidence / quality of life and simultaneously reduce health care visits or admissions. However, there is a large gap between the postulated and empirically demonstrated benefits of electronic Health Technologies. In addition, there is a lack of robust research on the risks of implementing these technologies and their cost-effectiveness has yet to be demonstrated, despite being frequently promoted by policymakers as if this was a given issue. In addition, the evidence-base for telehealth is not well-reported in peer reviewed journals and hence there continue to be difficulties experienced in convincing clinicians, hospital managers and stakeholders that investment in such technologies will enable reductions in other aspects of healthcare delivery over time. This project attempts to provide robust justification of the effectiveness of telerehabilitation by the implementation of a randomized controlled trial blindly assigning COPD patients to: i) a home care and telerehabilitation group remotely monitored by a specialised private health care centre (Filoktitis - group A) or ii) a hospital-based rehabilitation group managed at a regular base through weekly visits by personnel at a state University rehabilitation centre (group B). iii) A third group that receives usual care (group C: control group; i.e.: neither home monitoring nor hospital based rehabilitation) is also included.

NCT ID: NCT02615795 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease, COPD

Tele Health Monitoring Service for Patients With Chronic Obstructive Pulmonary Disease

Start date: March 2011
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of monitoring patients with chronic obstructive pulmonary disease (COPD) after a hospitalization for COPD exacerbation or pneumonia. The patients are randomized to receive either standard treatment and follow up, or standard treatment and follow up, plus tele monitoring of key clinical parameters and symptoms for six months.

NCT ID: NCT02614105 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Urinary Incontinence Amongst Women With Chronic Obstructive Pulmonary Disease

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

The primary aim of the study is to investigate whether pelvic floor muscle training or cough-suppression therapy reduces symptoms of urinary incontinence amongst women with chronic obstructive pulmonary disease grade 1-4 (mild to very severe disease).