To investigate the physical inflammation inhibition effects of EIL (Ectoin-Hydro-Complex) in subjects of the established SALIA-cohort and the preventive effects on lung function decline.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
36
Once daily inhalation of Ectoin Inhalation Solution
Once daily inhalation of Placebo Inhalation Solution
Institut für umweltmedizinische Forschung
Düsseldorf, Germany
Reduction of inflammatory markers considered to be indicative for the protective efficacy of EIL in pulmonary inflammation in COPD
Change of biomarkers in spautum, exhaled breath condensate and serum after treatment compared to baseline.
Time frame: Baseline and 28 days after treatment start
Vital signs
Time frame: Baseline and 28 days after treatment start
Reduction of lung function decline
Time frame: Baseline and 28 days after treatment start
Change in Quality of life
Time frame: Baseline and 28 days after treatment start
Need for rescue medication
Time frame: 28 days (during treatment phase)
Occurence of adverse events
Time frame: 28 days (during treatment phase)
Lung function parameters
Time frame: 28 days (during treatment phase)
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