Improvement of quality of life in patients with BO and establishment of a new third line therapy
Primary Objectives: Objective improvement of lung function, i.e.: * Improvement of SO2, pO2 or pCO2 in oxygen dependent or improvement of FiO2 in respiration dependent patients ≥ 20 % or * Reduction of oxygen need in oxygen dependent patients ≥ 1L O2/min with constant parameters at blood gas analysis (BGA) or * Improvement of obstructive parameters ≥ 20 % or * Improvement of lung function score (LFS) at least about one grade Improvement of lung function should be detectable at least by two consecutive examinations of lung function or BGA within at least four weeks. Secondary Objectives * Morphological improvement of BO/BOOP at CT scan * Reduction of steroids about at least 20 %
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Initial dose: 50µg s.c. three times/week, without fever \>38,5 dose increase: 50µg/m² BSA three times/week
University Hospital Regensburg
Regensburg, Germany
therapy response
Enhancement of therapy response from 15 % to 50 %
Time frame: 24 weeks
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