Effects of ROFLUMILAST on Subclinical Atherosclerosis in Chronic Obstructive Pulmonary Disease (COPD)

Chronic Obstructive Pulmonary Disease and Allied Conditions Clinical Trial

— ELASTIC  

Official title:

Effects of ROFLUMILAST on Markers of Subclinical Atherosclerosis In Stable COPD; the ELASTIC-trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01630200
• Other study ID #: ELASTIC2011
• Status: Completed
• Phase: Phase 4
• Start date: May 2012
• Est. completion date: January 2016

Study information

• Verified date: January 2019
• Source: LudwLudwig Boltzmann Institute for COPD and Respiratory Epidemiology
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chronic obstructive pulmonary disease is associated with a low grade systemic inflammatory process. Systemic inflammation is hypothesized to maintain cardiovascular morbidity and mortality in COPD. Early changes of vascular integrity can be detected via markers of subclinical atherosclerosis.

Selective Inhibition of phosphodiesterase subtype 4 describes a promising therapeutic option in COPD with beneficial impact on lung function and exacerbation rate. Moreover, an anti-inflammatory effect of phosphodiesterase-4 inhibition was confirmed by recent data.

The aim of this study is to assess the effects of the phosphodiesterase-4 inhibitor Roflumilast on firstly surrogates of subclinical atherosclerosis and secondly markers of systemic inflammation in the peripheral circulation of patients with stable chronic obstructive pulmonary disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: January 2016
• Est. primary completion date: January 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

• Over 40 years of age

• Smoking history of at least 10 pack years

• Chronic obstructive pulmonary disease at Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage II - IV diagnosed according to standard criteria.

• History of at least one COPD exacerbation requiring systemic corticosteroid treatment or hospitalisation in the previous year

Exclusion Criteria:

• Insufficient compliance to study medication (=70% of tablets used) during 4 weeks run-in period

• History of acute exacerbation 4 weeks prior to run-in period

• Diagnosis of alpha-1-antitrypsin deficiency

• Diagnosis of asthma

• Acute respiratory infections (e.g. pneumonia)

• Severe acute infectious diseases (e.g. active hepatitis, HIV)

• Lung cancer

• Bronchiectasis

• Interstitial lung disease

• Any other relevant lung disease

• Acute myocardial infarction

• Systolic left ventricular dysfunction

• Congestive heart failure New York Heart Association Functional Classification (NYHA) severity grade IV

• Haemodynamically significant cardiac arrhythmias or heart valve deformations

• Peripheral arterial occlusive disease

• Acute or chronic renal/hepatic failure

• Active malignancy

• Autoimmune disease

• Pregnant or breastfeeding women

• Women no using or not willing to use adequate contraceptive measures for the duration of the trial

• Hypersensitivity to study medication or placebo

• Severe psychiatric or neurological disorders or history of depression associated with suicidal ideation or behaviour

• Galactose intolerance, lactase insufficiency or glucose-galactose malabsorption

Related Conditions & MeSH terms

• Atherosclerosis
• Chronic Obstructive Pulmonary Disease and Allied Conditions
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Drug:
• Roflumilast
Roflumilast coated tablet, 500µg oral application, once daily in the morning
• Placebo
Placebo coated tablet (visually identical to 500µg Roflumilast tablet), oral application, once daily in the morning

Locations

Country	Name	City	State
Austria	Deparment for Respiratory and Critical Care Medicine, Otto Wangner Hospital	Vienna

Sponsors (2)

Lead Sponsor	Collaborator
LudwLudwig Boltzmann Institute for COPD and Respiratory Epidemiology	Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline in Carotid Femoral-Pulse Wave Velocity at Month 6	Carotid femoral-Pulse Wave Velocity (cf-PWV) will be measured non-invasively via applanation tonometry (AtCor Medical, Sydney, Australia). Wave propagation time will be calculated by the system software, using an ECG-gated reference frame. Aortic PWV is defined as the distance between two recording sites (i.e. common carotid- and femoral artery) divided by the wave propagation time.	baseline, month 6
Secondary	Change From Baseline in Reactive Hyperemia Index at Month 6	Endothelial dysfunction will be assessed by Flow Mediated Dilation via the Endopat device. This validated system measures the pulse wave amplitudes at the tip of both index fingers. The dominant arm will be occluded for 5 minutes by a sphygmomanometric cuff. After cuff deflation the pulse wave amplitude will be assessed to finally calculate the ratio of pulse wave amplitude before and after cuff-induced hyperemia. The so called reactive hyperemia index represents endothelial dysfunction at the level of conduit as well as resistance vessels.	baseline, month 6
Secondary	Change From Baseline in Augmentation Index at Month 6	The curve of the peripheral pressure wave will be recorded from the radial artery. Augmentation index (Aix) will be calculated from the generated central aortic pressure waveform via pulse wave analysis function. To correct for respective influences, Aix will be adjusted for a heart rate of 75 bpm. Appropriate intra observer validity will be assured via an operator index = 80.	baseline, month 6
Secondary	Change From Baseline in Matrix Metalloproteinase-9	Circulating levels of Matrix Metalloproteinase-9 (MMP-9) will be quantified from venous blood samples via Enzyme-linked Immunosorbent Assay	baseline, month 6
Secondary	Change From Baseline in Asymmetric Dimethylarginine at Month 6	Circulating levels of Asymmetric dimethylarginine (ADMA) will be quantified from venous blood samples via Enzyme-linked Immunosorbent Assay	baseline, month 6
Secondary	Change From Baseline in Tumor Necrosis Factor-alpha at Month 6	Circulating levels of Tumor Necrosis Factor-alpha (TNF-alpha) will be quantified from venous blood samples via Enzyme-linked Immunosorbent Assay	baseline, month 6
Secondary	Change From Baseline in Forced Expiratory Volume in 1 Second at Month 6	Forced Expiratory Volume in 1 second (FEV1) will be measured via standardized Spirometry	baseline, month 6
Secondary	Change From Baseline in 6-Minute Walk Test at Month 6	6-Minute Walk Test (6MWT) will be assessed to quantify functional exercise capacity following the standardized protocol of the American Thoracic Society	baseline, month 6
Secondary	Change From Baseline in COPD Assessment Test at Month 6	COPD Assessment Test (CAT) will be assessed to quantify patients disease related symptoms and to measure the impact of COPD on a patient's life, and how this changes over time. CAT is a standardised and validated patient questionaire comprising 8 distinct questions about different COPD-related symptoms. Each symptom is quantified by the patient on a numeric scale ranging from 0 to 5. Each symptom gives a number of points quantified as interval data without decimal places. The 8 different numbers of points are added to a total number expressed as the final points of the CAT score. The minimum achievable number of points is 0 and the maximum achievable number of points is 40. Higher values provide high symptoms and worse outcome, lower values provide low symptoms and better outcome.	baseline, month 6