University Grenoble Hospital
Grenoble, La Tronche, 38700, France
Location status: Recruiting
NCT Number: NCT03014609
The principal objective of the study is to measure parameters of inflammation, oxidative stress, and vascular, respiratory, and peripheral muscle function parameters, and identify parameters indicative of evolving cardiovascular risk (CVR) in COPD patients, using multivariate analysis.
Interested in participating?
Request Info18 year–85 year
All sexes
Observational
Grenoble, La Tronche, 38700, France
Location status: Recruiting
Reduced lung function is a major risk factor for cardiovascular mortality (CV), regardless of age, sex and history of smoking. Similarly, CV events are known causes of mortality in patients with chronic obstructive pulmonary disease (COPD). The investigators propose to determine the parameters influencing the evolution of CV risk in a cohort of COPD patients followed over 5 years. For this the investigators will study the role of inflammation, oxidative stress, and vascular, respiratory and peripheral muscle function parameters.
In order to study a sufficient number of patients the investigators propose to group data from two cohorts: a first cohort of 121 COPD patients that already exists (currently closed to inclusions but still undergoing follow-up (NCT00404430)) and a new cohort of 150, decompensated or not, COPD patients.
This study is of major scientific interest and will enable to obtain extremely important information to better understand COPD.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For patients with stable COPD:
For patients with decompensated COPD:
Exclusion criteria
Time frame: During 5 years since inclusion (once a year)
Measurement of pulse wave velocity (PWV), which reflects cardiovascular risk (CVR).
This measure will be performed at each visit (V1, V1 bis, V2, V3, V4, V5 and V6).
Time frame: During 5 years since inclusion
Determination of the relationship between exacerbations and the evolution of the PWV.
Time frame: During 5 years since inclusion (once a year)
Follow-up of exacerbations compared to new CV events (including myocardial infarction with or without ST segment elevation, ischemic stroke, unexplained sudden death at 5 years).
Time frame: During 5 years since inclusion (once a year)
Measurement of extent of pulmonary disease; exploration of peripheral muscle function; measurement of physical activity; measurements of endothelial function; measurement of cardiac function.
Time frame: During 5 years since inclusion (once a year)
Measurement of ambulatory arterial blood pressure during 24 hours
Time frame: At inclusion visit
Measurement of sleep disorders and Sleep Apnea Syndrome
Interested in participating?
Request InfoUniversity Hospital, Grenoble
Other
Cardiovascular Risk and Chronic Obstructive Pulmonary Disease (COPD)
Acronym: ECO-COPD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07384897
Bronchial Neoplasms, Carcinoma, Bronchogenic
Brussels, Belgium
View Trial DetailsNCT00435708
Chronic Disease, Chronic Obstructive Pulmonary Disease
Belfast, Co.Antrim, United Kingdom
View Trial DetailsNCT04448626
Atrophy, Chronic Disease
Montpellier, France
View Trial DetailsNCT01832961
Chronic Disease, Chronic Obstructive Pulmonary Disease
London, United Kingdom
View Trial Details