CVD-Cog trial
CerebroVascular Disease - Cognition


ISRCTN 14632228 / IRAS project ID 1011543
 Room S/D2116, Stroke Trials Unit
School of Medicine, University of Nottingham
Queen's Medical Centre, Derby Road
Nottingham NG7 2UH, United Kingdom
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  • Serious Adverse Events (SAEs) — we have a legal responsibility to collect all SAEs (including SARs/SUSARs) which all need to be reported during the trial period.
  • Please assess if expected according to RSI.  Expectedness should only be assessed in events that are thought to be possibly/probably/definitely related to the IMP.
  • Investigators have a legal responsibility to report applicable SAEs to the chief investigator without delay, within 24 hours.

Latest recruiting hospitals
Royal Cornwall Hospitals Trust, Truro, UK
Good Hope Hospital, Birmingham, UK
Derby Royal Hospital, Derby, UK
Luton and Dunstable University Hospital, Luton, UK
London North West, Middlesex, UK
  
Average time to randomisation (last 6 months)
# Days Hospital
1 10.0 London North West, Middlesex, UK
2 35.0 Derby Royal Hospital, Derby, UK
1 35.0 Luton and Dunstable University Hospital, Luton, UK
1 35.0 Good Hope Hospital, Birmingham, UK
1 35.0 Royal Cornwall Hospitals Trust, Truro, UK
Documents