Reduction of Corticosteroid Use in Outpatient Treatment of Exacerbated COPD (RECUT)
Pulmonary Disease, Chronic Obstructive, Adverse Effect of Glucocorticoids and Synthetic Analogues, Disease Exacerbation
About this trial
This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive focused on measuring Corticosteroid treatment, COPD, Primary Health Care, Randomized controlled trial
Eligibility Criteria
Inclusion Criteria:
- Informed Consent as documented by signature
- Age ≥40 years
- History of ≥10 pack-years of smoking (past or present smokers)
- Airway obstruction, defined as FEV1/FVC≤70%
Current acute exacerbation of COPD by clinical criteria, defined by the presence of at least two of the following:
- Change of baseline dyspnea
- Change of cough
- Change of sputum quantity or purulence
Exclusion Criteria:
- Diagnosis of asthma
- Initial necessity of hospitalization
- Women who are pregnant or breast feeding
- Premenopausal women with insufficient contraception and anamnestic risk for pregnancy
- Severe coexisting disease with life expectancy <6 months
- Diagnosis of tuberculosis
- Known severe immunosuppression or immunosuppression after solid organ or stem cell transplantation
- Inability to follow study procedures, e.g. due to language problems, psychological disorders, dementia, etc. of the participant
- Participation in another study involving an investigational drug
- Previous enrolment into the current study
Sites / Locations
- Kantonsspital BasellandRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Investigational treatment
Standard treatment
Patients included in the placebo group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for three days followed by two days of placebo.
Patients included in the control group are receiving systemic corticosteroid treatment (equivalent of 40mg prednisone daily) for five days as recommended in current guidelines.