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
National Hospital for Neurology & Neurosurgery, London, UK
Royal Derby Hospital, Derby, UK
Leighton Hospital, Crewe, UK
Queen's Medical Centre, Nottingham, 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
5 13.5 Royal Derby Hospital, Derby, UK
2 14.4 Queen's Medical Centre, Nottingham, UK
4 15.5 National Hospital for Neurology & Neurosurgery, London, UK
1 18.6 Leighton Hospital, Crewe, UK
1 19.1 Aberdeen Royal Infirmary, Aberdeen, UK
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