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Completed

NCT Number: NCT04481555

Eosinophil-guided Reduction of Inhaled Corticosteroids

Clinical trial on eosinophil-guided time-updated person-specific reduction of inhaled corticosteroid (ICS) therapy and prophylactic azithromycin therapy in patients with severe or very severe chronic obstructive pulmonary disease (COPD) receiving long-acting b-agonist (LABA) / long-acting muscarinic receptor antagonists (LAMA) / ICS treatment.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Aarhus University Hospital, Aarhus, Denmark

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About this study

Inhaled corticosteroid (ICS) treatment is recommended by Global Initiative for Obstructive Lung Disease (GOLD) for patients with frequent and/or servere exacerbations and blood eosinophils > 0.3 x 10^9 cells/L and in those with ≥ 0,1 x 109 cells blood-eosinophils and recurrent exacerbations while on bronchodilators. ICS treatment, however, is associated with side effects such as diabetes, osteoporosis and pneumonia which is costly for both patients and society. By studying the effects of a personalized, eoseosinophil-guided approach to direct ICS in COPD patients with frequent AECOPDs through a randomized clinical trial this study will examine the possibilities of reducing ICS overtreatment and thus ICS-related adverse events.

Long term ICS treatment is known for affecting the bacterial load in stable COPD patients. Azithromycin exerts multiple effects on the structure and composition of the lower airway microbiota and has anti-inflammatory effects. This study will, moreover, investigate whether an oral low-dose prophylactic treatment with Azithromycin 250 mg three times weekly can reduce the number of moderate-severe AECOPD and improves time alive and out of hospital.

This study is a randomized, double-blinded, multicentre, four-arm intervention clinical trial and is conducted based on the principles of good clinical practise (GCP).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • COPD (verified by a specialist in respiratory medicine + spirometry)
  • GOLD class E anytime within the last 2 years (corresponding to 2 ≥ AECOPD and/or ≥1 AECOPD leading to hospitalization during a 12 months period within the last 2 years) and/or FEV1<30%.
  • Treatment for last 4 weeks including LAMA, LABA and ICS
  • Informed consent

Exclusion criteria

  • Known asthma.
  • Male < 40 years.
  • Female <40 years, if non-menopausal (had menstruation within the last 12 months) conditioned by a negative urine HCG test
  • Severe mental illness which considerably complicates co-operation.
  • Language problems that considerably complicate co-operation.
  • Current treatment with systemic corticosteroids corresponding to > 5 mg prednisolone per day.
  • Systemic antibiotic treatment (if to participate in microbiota sub-study) or systemic corticosteroid treatment within 14 days (also prophylactic Azithromycin).
  • Contra-indication to treat with Azithromycin (as listed by the producer).
  • Non-bacterial exacerbation per investigator judgement in the last 3 months.

Treatment and study plan

Azithromycin

Drug

Prophylactic azithromycin treatment 250 mg three times weekly vs placebo

ICS

Drug

All patients will receive LABA/LAMA medication. The ICS medication will be switched on/off according to the most recent blood eosinophil count (at inclusion + every 3 months) vs continued LABA/LAMA/ICS treatment

Primary outcomes

  1. Exacerbations, hospital and death

    Time frame: 365 days

    Number of hospitalization-requiring exacerbations within 12 months and/or death within 365 days

Secondary outcomes

  1. Days alive, out of hospital

    Time frame: 365 days

    Days alive and out of hospital within 365 days after recruitment

  2. Deaths, uncontrolled AECOPD

    Time frame: 365 days

    Death or uncontrolled AECOPD tendency within 365 days

  3. Number of exacerbations

    Time frame: 365 days

    Number of moderate/severe exacerbation within 365 days

  4. Cumulative ICS dose

    Time frame: 365 days

    Cumulative dose of inhaled corticosteroids within 365 days

  5. Cumulative OCS dose

    Time frame: 365 days

    Cumulative dose of systemic corticosteroids within 365 days

  6. Change in FEV1

    Time frame: 365 days

    Change in lung function (ΔFEV1) from baseline to 365 days

  7. Change in blood eosinophils

    Time frame: 365 days

    Change in blood eosinophils from baseline to 365 days (eosinophilic trajectories)

  8. Diabetes mellitus

    Time frame: 365 days

    New diagnosis of diabetes mellitus within 365 days

  9. Change in HbA1c

    Time frame: 365 days

    Change in HbA1c from baseline to 365 days

  10. Number of antibiotic requiring infections

    Time frame: 365 days

    Antibiotic-requiring infections within 365 days

  11. Microbiota, abundance and diversity

    Time frame: 365 days

    Difference in respiratory microbiota abundance and diversity from baseline to 12 months between treatment arms

  12. Microbiota, immunological profile

    Time frame: 365 days

    Difference in immunological profile including cytokines and chemokines in the upper airways from baseline to 12 months between treatment arms

  13. Change in CAT score

    Time frame: 365 days

    Change in COPD-related quality of life (Based on COPD Assessment Test - CAT) from baseline to 365 days

  14. Change in MRC dyspnoea score

    Time frame: 365 days

    Number who progress to MRC -dyspnea score from < 3 to ≥3 anytime during follow-up (assessed every 3 months).

  15. Number of non-invasive ventilation (NIV) or intensive care admissions or death

    Time frame: 365 days

    Number of admission requiring non-invasive ventilation (NIV) treatment or admissions to intensive care within 365 days

  16. Mortality

    Time frame: 365 days

    Mortality within 365 days

Sponsors and collaborators

Lead sponsor

Chronic Obstructive Pulmonary Disease Trial Network, Denmark

Other

Registry information

Acronym: COPERNICOS

Important dates

Study start
2021
Primary completion
2024
Study completion
2025
First posted
Jul 22, 2020
Registry last updated
Jan 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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