Peripheral Endothelial Function in COPD Patients (endothBPCO)
Primary Purpose
Chronic Obstructive Pulmonary Disease
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
COPD patients
Sponsored by
About this trial
This is an interventional basic science trial for Chronic Obstructive Pulmonary Disease focused on measuring endothelial function, COPD, pulmonary function
Eligibility Criteria
Inclusion Criteria:
- COPD : FEV1/FVC < 70%
- Smokers or ex-smokers ( ≥ 10 pack-years)
- No COPD exacerbation in the last three months
- No history of asthma and no respiratory allergy
Exclusion Criteria:
- Pregnant or nursing women
- Treatment with pulmonary vasodilators
- Patients with a significant acute disease. A significant disease is defined as a disease which, in the opinion of the investigator, may influence the results of the trial.
Sites / Locations
- Hôpital Saint-Antoine
- Hôpital Foch
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
COPD patients
Arm Description
measure of endothelial function with EndoPAT® in COPD patients
Outcomes
Primary Outcome Measures
measure of reactive hyperemia-peripheral artery tone index
measure of reactive hyperemia-peripheral artery tone index
Secondary Outcome Measures
measure of Forced expiratory flow in one second
measure of Forced expiratory flow in one second
measure of forced vital capacity
measure of forced vital capacity
measure of expiratory flow between 25% and 75% (FEF25-75%).
measure of expiratory flow between 25% and 75% (FEF25-75%).
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02593357
Brief Title
Peripheral Endothelial Function in COPD Patients
Acronym
endothBPCO
Official Title
Assessment of a Peripheral Endothelial Dysfunction in COPD (Chronic Obstructive Pulmonary Disease)
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
December 17, 2012 (Actual)
Primary Completion Date
July 6, 2017 (Actual)
Study Completion Date
August 17, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hopital Foch
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of the study is to assess the peripheral endothelial function in adult COPD (chronic obstructive pulmonary disease) patients and the relationship between the peripheral endothelial function and the pulmonary function.
Detailed Description
The primary criteria is the peripheral endothelial function that will be assessed by the measure of flow-mediated dilation (reactive hyperemia-peripheral artery tone index). The pulmonary function will be assessed by the measures of the FEV1 (forced expiratory volume in one second), the forced vital capacity (FVC) and the expiratory flow between 25% and 75% (FEF25-75%). The relationship between these parameters of the pulmonary function and the peripheral endothelial function will be analyzed. In addition, a relationship between peripheral endothelial function and the severity of COPD (classification according to GOLD (Global Initiative for Chronic Obstructive Lung Disease) 2010 and GOLD 2011 and the COPD assessment test, the cardiovascular risk factors (SCORE INdex) and the smoker status will be also assessed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
endothelial function, COPD, pulmonary function
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
137 (Actual)
8. Arms, Groups, and Interventions
Arm Title
COPD patients
Arm Type
Experimental
Arm Description
measure of endothelial function with EndoPAT® in COPD patients
Intervention Type
Device
Intervention Name(s)
COPD patients
Intervention Description
measure of peripheral endothelial function by the reactive hyperemia-peripheral artery tone index with a specific device (EndoPAT®)
Primary Outcome Measure Information:
Title
measure of reactive hyperemia-peripheral artery tone index
Description
measure of reactive hyperemia-peripheral artery tone index
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
measure of Forced expiratory flow in one second
Description
measure of Forced expiratory flow in one second
Time Frame
day 1
Title
measure of forced vital capacity
Description
measure of forced vital capacity
Time Frame
day 1
Title
measure of expiratory flow between 25% and 75% (FEF25-75%).
Description
measure of expiratory flow between 25% and 75% (FEF25-75%).
Time Frame
day 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
COPD : FEV1/FVC < 70%
Smokers or ex-smokers ( ≥ 10 pack-years)
No COPD exacerbation in the last three months
No history of asthma and no respiratory allergy
Exclusion Criteria:
Pregnant or nursing women
Treatment with pulmonary vasodilators
Patients with a significant acute disease. A significant disease is defined as a disease which, in the opinion of the investigator, may influence the results of the trial.
Facility Information:
Facility Name
Hôpital Saint-Antoine
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
Hôpital Foch
City
Suresnes
ZIP/Postal Code
92150
Country
France
12. IPD Sharing Statement
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Peripheral Endothelial Function in COPD Patients
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