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The prevalence of DRPs in patients will be determined at baseline and after 6 months in both groups.
The following special analyses will be determined at baseline in all selected participants: serum anti-PLA2R antibodies (ELISA, Euroimmun AG, Luebeck, Germany), the number of T cells CD4+, CD8+, CD4+/CD8+ cell ratio, and CD19+ cells.
The measurement of work ability will be determined at baseline and after six months with the first three items of the Work Ability Index (wai)[ 21]: 1) current work ability compared with the lifetime best; 2) perceived work ability with respect to physical demands; and 3) perceived work ability with respect to mental demands.
The newly approved labeling states that serum glutamic pyruvic transaminase (SGPT)/ALT and serum glutamic oxaloacetic transaminase (SGOT)/AST levels should be determined at baseline, as well as periodically (ie, every two to four weeks) for the first six months of therapy.
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Microsphere blood flows were determined at baseline, during occlusion, after reperfusion, and before euthanasia.
Neurologic impairment score and electromyogram were determined at baseline and 12 months.
Plasma thromboxane B2 level was determined at baseline and 10 minutes after protamine injection.
Plasma concentrations of TNF-α, IL-6, and IL-1β were determined at baseline and at 3 h after declamping.
Glycaemic control and cardiovascular risk factors were determined at baseline and at the end of the treatment period.
Serum SHBG and fT levels were determined at baseline and after first and second years of treatment.
Patient-rated wrist and hand evaluation (PRWHE) scores were determined at baseline (before arthroscopy) and one year after arthroscopy.
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