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Effect of Roflumilast on Quality of Life, Lung Function and Mucus Properties in Patients With Bronchiectasis

Effect of Roflumilast on Quality of Life, Lung Function and Mucus Properties in Patients With Non-cystic Fibrosis Bronchiectasis: a Cross-over, Unicentric, Double-blind and Placebo-controlled Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03988816
Enrollment
30
Registered
2019-06-17
Start date
2019-12-06
Completion date
2020-12-31
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiectasis Adult

Keywords

bronchiectasis, lung function, quality of life, mucus properties

Brief summary

Although relatively common, bronchiectasis is considered an orphan disease as there is little evidence for adequate treatment, most of the therapeutic options are extrapolated from studies with patients with chronic obstructive pulmonary disease (COPD) or cystic fibrosis (CF). Inhaled bronchodilators and corticosteroids should be used as a therapeutic test and maintained if there is improvement of symptoms or lung function. There is no evidence to justify the use of mucolytic agents for these patients. The treatment with greater evidence is the use of macrolides, especially azithromycin. A meta-analysis published in 2014 showed that there was a reduction in the number of exacerbations, an improvement in the quality of life and a reduction in the decrease in FEV1. However, studies have shown conflicting results regarding quality of life and pulmonary function. Roflumilast is a phosphodiesterase-4 inhibitor with an anti-inflammatory effect in vitro and in vivo due to the inhibition of cyclic adenosine monopostat breakdown (cAMP) to its inactive phosphodiesterase form. As this enzyme is expressed in high concentrations in leukocytes and other inflammatory cells responsible for the pathogenesis of pulmonary diseases such as COPD, it has been studied and used for this disease. COPD is characterized by a chronic inflammatory process of the airways, predominantly neutrophils and high levels of proinflammatory cytokines related to this cell, such as interleukin-8, neutrophil elastase, tumor necrosis factor (TNF) alpha and E-selectin. The REACT study showed that roflumilast prevents moderate and severe infectious exacerbations in addition to improved lung function in patients with COPD who continue to exacerbate despite the use of combined bronchodilator and inhaled corticosteroid therapy. Since bronchiectasis and COPD are chronic inflammatory diseases, they present similar inflammatory processes, with neutrophil as the main inflammatory cell, it is expected that the use of roflumilast also has an anti-inflammatory effect in bronchiectasis. In addition, since bronchiectasis is a disease with poor evidence for pharmacological treatment, it is necessary to search for new therapeutic possibilities.

Interventions

DRUGRoflumilast

500Mcg Tab, once daily

DRUGPlacebo oral tablet

once daily

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Placebo-controlled

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years; * Diagnosis of bronchiectasis by chest tomography; * FEV1 \<60% of predicted; * History of chronic bronchitis (chronic cough and sputum for at least 3 months in the last 2 years); * 2 or more infectious exacerbations in the last year (defined as worsening of cough and / or dyspnoea and / or decreased general condition, increased quantity and purulence of sputum that required systemic antibiotic use (oral or intravenous).

Exclusion criteria

* Hemoptysis in the last 6 months (significance at the discretion of the investigator); * Current or prior smoking if \> 10 pack-years; * FEV1 \< 30% of predicted; * Known allergy to roflumilast; * Pulmonary exacerbation present or occurring in the last 4 weeks; * Child B or C cirrhosis; * Active cancer (except basal cell carcinoma); * Severe heart failure; * Depression associated with suicidal ideation; * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life questionnaire12 weeksTo evaluate the impact of roflumilast on the quality of life of patients with bronchiectasis through the Saint George Respiratory Questionnaire (SGRQ).

Secondary

MeasureTime frameDescription
Other tools for quality of life12 weeksTo evaluate the impact of roflumilast on quality of life using the questionnaires Leicester, Quality of Life Questionnaire-Bronchiectasis (QOL-B) Bronchiectasis Health Questionnaire (BHQ)
Dyspnea12 weeksTo evaluate the impact of roflumilast on severity of dyspnea as measured by the COPD Assessment Test (CAT)
Lung function12 weeksTo evaluate the impact of roflumilast on lung function measured by forced expiratory volume at one second (FEV1)
Adverse events12 weeksTo evaluate the safety of roflumilast assessed through the incidence of adverse events

Countries

Brazil

Contacts

Primary ContactRodrigo A Athanazio, MD, PhD
rathanazio@yahoo.com.br+55 11 2661-5000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026