Chronic Obstructive Pulmonary Disease
Conditions
Keywords
Post-bronchodilator FEV1<70% reference, Chronic bronchitis, Presence of estavlished CVD,, CVD equivalent or diabetes mellitus
Brief summary
REVASC is a randomized, double-blind, placebo-controlled study which will involve 150 patients with chronic bronchitis and COPD diagnosed cardiovascular disease. The recruitment period beginimg in the coming weeks, will last nine months. Patients included in the study will receive treatment for three months with roflumilast 500 mg (75 patients) or placebo (75 patients) in a randomized manner. The CIBERES, as promoter of this study is expected to release final results for the third quarter of 2013. Eight centers in Madrid will be involved in this clinical trial: Fundación Jiménez Díaz, Hospital La Princesa, Hospital Gregorio Maranon Hospital Clinico San Carlos, Hospital La Paz, Hospital Ramón y Cajal Hospital Doce de Octubre and Hospital Puerta del Hierro. Roflumilast is a potent phosphodiesterase-4 inhibitor (PDE4). Its clinical efficacy has been studied in an extensive clinical program involving over 12,000 patients with COPD. In these studies, roflumilast (in combination with long-acting bronchodilators) reduced the number of exacerbations and improved lung function, especially in those patients with associated chronic bronchitis.
Interventions
DRUGRoflumilast 500
Roflumilast 500 mcg , 12 weeks of treatment
DRUGPlacebo
Placebo 500 mcg , 12 weeks of treatment
Sponsors
Spanish Research Center for Respiratory Diseases
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
55 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Signed informed consent * 55-75 years of age * Current and former smokers \>20 cigarettes pack-yr (if former smokers withdrawn \>1 year) * Diagnosis COPD (GOLD criteria1 for more than a year before V0) * Presence of chronic bronchitis (cough and/or expectoration for more that 3 months/yr for more than 2 consecutive yrs. in the absence of other potential cause) * Post-bronchodilator FEV1\<70% reference * Presence of established CVD, CVD equivalent or diabetes mellitus * Presence of chronic systemic inflammation, determined on: 1. Serum CRP ≥ 2 and \< 10 mg/l or 2. Serum fibrinogen \> 518 mg/dl and Leucocytes \> 8,6\*106 /mm3
Exclusion criteria
* Episode of COPD exacerbation and/or COPD treatment change during the last 2 months before V0 * History of asthma, significant residual lung lesions or bronchiectasis on chest x-ray * Apnea-hypopnea syndrome * Poorly controlled CVD risk factors (Table 2) and/or change in their treatment during the last 3 months before V0 * Clinically significant cardiac arrhythmias or valve disease * Severe concomitant immunological, inflammatory, infectious or neoplastic diseases * Moderate or severe hepatic insufficiency (B or C class, following Child-Pugh scale) * Severe neurologic and/or psychiatric disorder, including depression with suicidal ideas * Alcohol and/or drug abuse during the last 12 months before V0 * Hypersensitivity to roflumilast or to any of its excipients * Pregnancy or potential pregnancy * Participation in other clinical trial during the last 30 days before V0 * Language difficulties to follow the instructions of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endotelial function | 12 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Arterial siffness | 12 weeks |
| Serum and plasma inflammation markers: (CRP, fibrinogen, leucocytes, interleukin (IL)-8, IL-6, IL-10, tumor necrosis factor alpha (TNFα), sICAM-1, MCP-1, PARC/CCL-18) | 12 weeks |
| Serum oxidatrive stress markers: MPO, TRX | 12 weeks |
| Serum endothelial dysfunction markers:TWEAKs, FasL, ADMA | 12 weeks |
Countries
Spain
Contacts
Primary ContactÀlvar Agustí
Backup ContactPaloma Vaquer
Outcome results
None listed