“…A plethora of medical treatment options to attenuate vasospasm, such as statins, corticosteroids, clazosentan, milrinone, magnesium sulfate, fasudil hydrochloride, cilostazol and edaravone, has been tested in both, experimental and clinical settings; however, with exemption of one single agent, the calcium channel antagonist nimodipine, no systemic medical therapy has shown a robust and reproducible effect on functional outcome in these patients [ 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 ]. Therefore, in most centers, enteral administration of nimodipine is part of the standard treatment protocol in order to prevent vasospasm; however, different routes of administration including parenteral intravenous administration, intrathecal administration via external ventricular drainage and intracisternal administration via stereotactically placed catheters have been used and tested; yet, these alternative methods of administration remain to be of experimental character [ 16 , 17 , 18 , 19 , 20 , 21 , 22 ]. Furthermore, nimodipine has been administered intraarterially as a measure of local vasodilative rescue therapy in cases of symptomatic delayed cerebral vasospasm [ 17 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 ].…”