Table 1.
Measures | Baseline | Day 2 | Day 14 | Day 30 | Day 60 | Day 90 |
Demographics | x | |||||
History of present illness | x | |||||
mRS | x | x | x | x | x | x |
History | x | |||||
Medication | x | x | x | x | x | |
NIHSS | x | x | x | x | ||
Head CT | x | |||||
Head MRI | x | |||||
ASPECT | x | |||||
Laboratory examination∗ | x | x | ||||
Electrocardiograph | x | |||||
Inclusion and exclusion criteria | x | |||||
Informed consent | x | |||||
Randomisation | x | |||||
Injection | x | |||||
Compliance | x | x | x | x | ||
Special laboratory test | x | x | x | |||
TOAST classification | x | |||||
OCSP classification | x | |||||
EQ-5D | x | x | x | |||
MMSE | x | x | ||||
MoCA | x | x | ||||
Soft capsules | x | |||||
AE/SAE | x | x | x | x | x |
*Including at least test of blood glucose, blood routine examination (count of platelet), and renal and liver function (alanine transaminase, aspartate aminotransferase and creatinine).
AE, adverse event; ASPECT, Alberta Stroke Program Early CT Score; EQ-5D, EuroQol 5D; MMSE, Mini-Mental State Examination; MoCA, Montreal Cognitive Assessment; mRS, modified Rankin Scale; NIHSS, National Institutes of Health Stroke Scale; OCSP, Oxfordshire Community Stroke Programme; SAE, serious adverse event; TOAST, Trial of Org 10172 in Acute Stroke Treatment.