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Participation levels in the baseline and follow-up assessments were different for each of the outcome variables.
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Reaction products and microstructures of AAMs are different from ordinary Portland cement (OPC), therefore the corrosion mechanisms and assessments are different.
Owing to the loss to follow-up, the number of participants at both assessments was different.
As Table 2 shows, the candidates taking both assessments are different from the more typical candidates taking a single assessment.
Length of stay in hospital and hence length of time between assessments was different for each patient.
The research nurse responsible for follow-up assessments was different to the nurse who performed randomisation, and data entry was undertaken by trial administrators blinded to allocation.
Moreover, the timing of assessments was different between the two studies, with most children in the earlier study infected with malaria at the time of measles immunisation.
The timing of safety assessments was different between the two treatments arm (every 2 weeks in the FOLFIRI+Bev arm and every 3 weeks in the CAPIRI+Bev arm).
The criteria for the group and self-assessments were different, so the assessments did not even need to correlate well.
Investigators who performed the neurological outcome assessment were different from those who administered the FREMS or placebo treatment.
Baseline score and score at last assessment were different for both discharged patients and defaulters (p < 0.001).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com