25
Participants
Start Date
December 22, 2022
Primary Completion Date
December 31, 2026
Study Completion Date
February 28, 2027
Empagliflozin 25 MG
Patients who fulfill the inclusion criteria will receive an intravenous dose of 1.0-1.5 mg/kg of furosemide (≤120 mg) and urine output will be monitored for three hours. Those with a urine output \< 300 ml in the first two hours post furosemide administration will receive a single oral dose of 25 mg of empagliflozin. Two hours after taking empagliflozin, patients will receive a second intravenous dose of 1.0-1.5 mg/kg of furosemide with another timed urine collection at three hours. Empagliflozin will then be continued daily for five days or until hospital discharge, unless the treating physician considers this not to be clinically appropriate.
RECRUITING
Research Institute of the McGill University Health Center, Montreal
McGill University Health Centre/Research Institute of the McGill University Health Centre
OTHER