21
Participants
Start Date
August 1, 2025
Primary Completion Date
May 1, 2028
Study Completion Date
December 1, 2028
Adrenomedullin
The participants will receive continuous intravenous infusion of 20 mL of 19.9 pmol/kg/min adrenomedullin over 20 minutes.
Placebo
The participants will receive a continuous intravenous infusion of 20 mL of placebo (isotonic saline) over 20 minutes.
RECRUITING
Rigshospitalet-Glostrup, Glostrup Municipality
Danish Headache Center
OTHER