Chronic Obstructive Pulmonary Disease Clinical Trial
— ECO-COPDOfficial title:
Cardiovascular Risk and Chronic Obstructive Pulmonary Disease (COPD)
NCT number | NCT03014609 |
Other study ID # | 38RC16.245 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 9, 2017 |
Est. completion date | December 2029 |
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.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | December 2029 |
Est. primary completion date | November 2029 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | Inclusion Criteria: For patients with stable COPD: - Men or women aged 18 to 85 - FEV1/FVC < 70% or proven BPCO - Patients who have given their free and informed consent in writing For patients with decompensated COPD: - Men or women aged 18 to 85 - FEV1/FVC < 70% or proven BPCO - At the time of acute respiratory failure (ARF), when admitted to hospital: - Respiratory rate > 25 cycles per minute - PaCO2 > 45 mmHg - blood pH < 7.35 - When included in the study: - pH > 7.33 at the end of ARF, 2 days in a row, or 3 to 7 days post-D1 decompensation (admission to the hospital) - Fever < 38.5°C - Patients who have given their free and informed consent in writing Exclusion Criteria: - Obvious evolving infection or CRP > 100 mg/L - Cardiac decompensation considered the main cause of decompensation or chronic heart failure with LVEF < 45% - Evolving neoplasia - On antioxidants: N-acetyl-cysteine, selenium, vit. C, vit. E - Pregnant or nursing women - Patients under tutorship or curatorship - Patients participating in a drug clinical research study - Patients not affiliated to the French social security system (or equivalent) - Patients deprived of liberty or hospitalized without consent. |
Country | Name | City | State |
---|---|---|---|
France | University Grenoble Hospital | Grenoble | La Tronche |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Grenoble |
France,
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* Note: There are 29 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of the pulse wave velocity (PWV) | 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). |
During 5 years since inclusion (once a year) | |
Secondary | Monitoring of COPD exacerbations compared to evolution of PWV | Determination of the relationship between exacerbations and the evolution of the PWV. | During 5 years since inclusion | |
Secondary | Relationship between the new cardiovascular (CV) events and the evolution of the PWV. | 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). | During 5 years since inclusion (once a year) | |
Secondary | Correlations between the parameters of severity of pulmonary disease and physical activity. | Measurement of extent of pulmonary disease; exploration of peripheral muscle function; measurement of physical activity; measurements of endothelial function; measurement of cardiac function. | During 5 years since inclusion (once a year) | |
Secondary | Prevalence of nocturnal "non-dipping" of blood pressure during COPD. | Measurement of ambulatory arterial blood pressure during 24 hours | During 5 years since inclusion (once a year) | |
Secondary | Impact of sleep disorders and sleep apnea syndrome on the evolution of CVR during COPD. | Measurement of sleep disorders and Sleep Apnea Syndrome | At inclusion visit |
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