21
Participants
Start Date
March 21, 2022
Primary Completion Date
July 7, 2022
Study Completion Date
July 7, 2022
Levcromakalim
Study participants will be allocated to receive continuous intravenous infusion of 0.05 mg/min (20 ml of 50 mg/ml) levcromakalim.
Placebo
Study participants will be allocated to receive continuous intravenous infusion of 20 mL placebo (isotonic saline).
Danish Headache Center, Copenhagen
Danish Headache Center
OTHER