ReCAST-3 trial
Remote ischaemic Conditioning After Stroke Trial 3


ISRCTN 63231313
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Room S/D2108, 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 occurring within the first 20 days after randomisation (including SADEs/USADEs/fatal SAEs).
     
  • Please remember that all fatal SAEs and safety outcome events – cerebrovascular events, ACS, AKI, systemic embolism (e.g. ischaemic limb/bowel) and/or neurovascular limb compromise – need to be reported, even those after the first 20 day period, until the final day 90 follow-up.
  • Investigators have a legal responsibility to report applicable SAEs to the chief investigator without delay, within 24 hours.

Latest recruiting hospitals
Royal Derby Hospital, Derby, UK
Leighton Hospital, Crewe, UK
Queen's Medical Centre, Nottingham, UK
National Hospital for Neurology & Neurosurgery, London, UK
Aberdeen Royal Infirmary, Aberdeen, UK
Morriston Hospital, Swansea, UK
  
Average time to randomisation (last 6 months)
# Hours Hospital
1 4.9 Morriston Hospital, Swansea, UK
3 13.9 National Hospital for Neurology & Neurosurgery, London, UK
5 14.2 Royal Derby Hospital, Derby, UK
2 14.4 Queen's Medical Centre, Nottingham, UK
1 18.6 Leighton Hospital, Crewe, UK
1 19.1 Aberdeen Royal Infirmary, Aberdeen, UK
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