Clinical Trials Directory

Trials / Completed

CompletedNCT02593357

Peripheral Endothelial Function in COPD Patients

Assessment of a Peripheral Endothelial Dysfunction in COPD (Chronic Obstructive Pulmonary Disease)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
137 (actual)
Sponsor
Hopital Foch · Academic / Other
Sex
All
Age
40 Years – 75 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICECOPD patientsmeasure of peripheral endothelial function by the reactive hyperemia-peripheral artery tone index with a specific device (EndoPAT®)

Timeline

Start date
2012-12-17
Primary completion
2017-07-06
Completion
2017-08-17
First posted
2015-11-02
Last updated
2018-10-03

Locations

2 sites across 1 country: France

Source: ClinicalTrials.gov record NCT02593357. Inclusion in this directory is not an endorsement.

Peripheral Endothelial Function in COPD Patients (NCT02593357) · Clinical Trials Directory