71
Participants
Start Date
April 11, 2018
Primary Completion Date
October 31, 2021
Study Completion Date
December 31, 2021
Propranolol
Patients randomized to the experimental arm will receive propranolol on top of standard recommended treatment for CCM. Initial oral dose of 40 mg bid will be uptitrated to 80 mg bid in the absence of excessive bradycardia or hypotension. Doses as low as 10 mg bid and up to 160 mg bid, 20 to 320mg daily, are acceptable according to tolerability.
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan
Fond. IRCCS Ist. Naz. Neurologico Carlo Besta, Milan
ASST Grande Ospedale Metropolitano Niguarda, Milan
IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo
"IRCCS Centro Neurolesi Bonino Pulejo", Messina
"Fondazione Policlinico Universitario A. Gemelli", Roma
IFOM ETS - The AIRC Institute of Molecular Oncology
OTHER
Mario Negri Institute for Pharmacological Research
OTHER