Peripheral Endothelial Function in COPD Patients
endothBPCO
Assessment of a Peripheral Endothelial Dysfunction in COPD (Chronic Obstructive Pulmonary Disease)
1 other identifier
interventional
137
1 country
2
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable chronic-obstructive-pulmonary-disease
Started Dec 2012
Longer than P75 for not_applicable chronic-obstructive-pulmonary-disease
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 17, 2012
CompletedFirst Submitted
Initial submission to the registry
October 16, 2015
CompletedFirst Posted
Study publicly available on registry
November 2, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 6, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
August 17, 2017
CompletedOctober 3, 2018
October 1, 2018
4.6 years
October 16, 2015
October 1, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
measure of reactive hyperemia-peripheral artery tone index
measure of reactive hyperemia-peripheral artery tone index
Day 1
Secondary Outcomes (3)
measure of Forced expiratory flow in one second
day 1
measure of forced vital capacity
day 1
measure of expiratory flow between 25% and 75% (FEF25-75%).
day 1
Study Arms (1)
COPD patients
EXPERIMENTALmeasure of endothelial function with EndoPAT® in COPD patients
Interventions
measure of peripheral endothelial function by the reactive hyperemia-peripheral artery tone index with a specific device (EndoPAT®)
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Hopital Fochlead
Study Sites (2)
HĂ´pital Saint-Antoine
Paris, 75012, France
HĂ´pital Foch
Suresnes, 92150, France
Related Publications (50)
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PMID: 16171272BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 16, 2015
First Posted
November 2, 2015
Study Start
December 17, 2012
Primary Completion
July 6, 2017
Study Completion
August 17, 2017
Last Updated
October 3, 2018
Record last verified: 2018-10