MACE-ICH trial
MAnnitol for Cerebral oEdema after IntraCerebral Haemorrhage


EudraCT 2022-000283-22
Twitter
Room S/D2105, Stroke Trials Unit
School of Medicine, University of Nottingham
Queen's Medical Centre, Derby Road
Nottingham NG7 2UH, United Kingdom
Please log in if you need the MACE-ICH emergency contact numbers. The recruitment total for the trial to date is: 13

Login using the investigator ID, password issued to you by the

If you have forgotten your login details then please click here.

MACE-ICH investigator ID:
Password:

Please ensure that your web browser has both cookies and JavaScript enabled.

  • Serious Adverse Events (SAEs) — we have a legal responsibility to collect all SAEs occurring within the first 28 days after randomisation (including SARs/SUSARs/fatal SAEs).
  • Please remember that fatal SAEs and safety outcome events – thrombophlebitis, hyper-/hyponatraemia, pulmonary oedema, hypotension and renal impairment – need to be reported until the final month 6 follow-up, even if this is after 28 days.
  • Investigators have a legal responsibility to report applicable SAEs to the chief investigator without delay, within 24 hours.

Latest recruiting hospitals
Queen's Medical Centre, Nottingham, UK
Aberdeen Royal Infirmary, Aberdeen, UK
 
Average time to randomisation (last 6 months)
# Hours Hospital
11 19.5 Queen's Medical Centre, Nottingham, UK
2 25.5 Aberdeen Royal Infirmary, Aberdeen, UK
Documents