| Day 1 | Day 2 | Day 3 | Day 4 | Day 5 | Day 6 | Day 7 |
---|---|---|---|---|---|---|---|
Eligibility assessed by paramedic from routine clinical data | x | Â | Â | Â | Â | Â | Â |
Study discussed and verbal informed consent/assent obtained by paramedic | x | Â | Â | Â | Â | Â | Â |
Randomisation | x | Â | Â | Â | Â | Â | Â |
Further study information provided and written informed consent/assent obtained by hospital research team | x | Â | Â | Â | Â | Â | Â |
Appropriateness to continue study medication reviewed by hospital team | x | Â | Â | Â | Â | Â | Â |
Review of medical records to collect baseline stroke details and medical history | X | Â | Â | Â | Â | Â | Â |
Blood pressure measurements | x | x | x | Â | Â | Â | x |
National Institute of Health Stroke Scale | x | Â | x | Â | Â | Â | x |
Barthel ADL Index (pre-stroke) | x | Â | Â | Â | Â | Â | Â |
Barthel ADL Index (post-stroke) | Â | Â | Â | Â | Â | Â | x |
Modified Rankin Scale (pre-stroke) | x | Â | Â | Â | Â | Â | Â |
Modified Rankin Scale (post-stroke) | Â | Â | Â | Â | Â | Â | x |
Blood test for renal function | Â | Â | Â | Â | Â | Â | x |
Review of medical records to record concomitant blood pressure medications | Â | Â | Â | Â | Â | Â | x |
Treatment with study medication | x | x | x | x | x | x | x |
Review of study medication dosage | x | Â | Â | Â | Â | Â | Â |
Adverse Events | x | x | x | x | x | x | x |