200
Participants
Start Date
August 1, 2024
Primary Completion Date
October 1, 2025
Study Completion Date
October 1, 2026
Fasudil
A ROCK inhibitor approved for treating vasospasms following subarachnoidal bleeding in Japan and China. Dosage: Participants will undergo a 2-week titration period at 60 mg daily before escalating to a maintenance dose of 120 mg daily.
Placebo
Placebo tablets that look identical to the fasudil tablets and will follow the same dosing schedule as participants receiving fasudil.
NOT_YET_RECRUITING
University Hospital of North Norway, Tromsø
NOT_YET_RECRUITING
Akershus Hospital:, Oslo
NOT_YET_RECRUITING
Haugesund Hospital, Haugesund
RECRUITING
Stavanger University Hospital, Stavanger
NOT_YET_RECRUITING
St. Olavs Hospital:, Trondheim
ENROLLING_BY_INVITATION
Haraldsplass Deaconess Hospital, Bergen
University of Exeter
OTHER
Helse Fonna
OTHER
St. Olavs Hospital
OTHER
University Hospital, Akershus
OTHER
Haraldsplass Deaconess Hospital
OTHER
Helse Stavanger HF
OTHER_GOV