40
Participants
Start Date
October 31, 2025
Primary Completion Date
October 31, 2026
Study Completion Date
October 31, 2026
Eplerenone
"Participants will receive eplerenone 25 mg once daily or every other day, based on baseline potassium levels, eGFR, systolic blood pressure, and concomitant use of weak or moderate CYP3A4 inhibitors.~The study will implement a safety protocol with predefined procedures for managing significant hyperkalemia, worsening renal function, and hypotension. These will include temporary or permanent dose reduction or discontinuation of eplerenone, and, if necessary, administration of the potassium binder sodium zirconium cyclosilicate (SZC, Lokelma®)."
Department of Cardiology, Danderyd Hospital, Karolinska Institutet, Stockholm
Karolinska Institutet
OTHER