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The baseline visit will be done and then the patient will be scheduled for the next visit.
Slope values in subjects with versus without preeclampsia/eclampsia/HELLP syndrome within 4 weeks after the baseline visit will be described by descriptive statistics and illustrated by box-plot graphs.
Patients with a history of COPD for at least 12 months, associated with chronic productive cough for at least three months, in each of the two years prior to baseline visit will be recruited into the study.
In addition, the number and proportion of patients in both the rituximab and placebo groups who achieve a reduction in either oral dryness or fatigue >30% between the end of study visit (week 48) and the baseline visit will be summarised.
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Through the CEKOL collaboration [ 17] the blood samples collected during the baseline visits will be analysed for SP-D and MFAP4 levels at the Institute of Medical Biology, University of Southern Denmark, using the funding already obtained.
The baseline home visit will be followed up by phone interviews one and two years later.
Given the logistics of training patients within a nocturnal dialysis program, randomization will occur at one time point for patients willing to enter the study; however, patient entry into the study (i.e. the baseline study visit) will be staggered over time to facilitate NHD training in an orderly fashion.
At baseline, a home visit will be scheduled.
Symptoms and Syndromes from the E-MOSAIC software between baseline and after last study visit will be evaluated.
For all analyses, assessments performed at the first outpatient visit will be taken as baseline.
EPDS score taken at the home visit will be used as the baseline score in analyses.
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