10
Participants
Start Date
July 10, 2024
Primary Completion Date
July 10, 2025
Study Completion Date
September 1, 2025
Semaglutide
"10 overweight patients with heart failure will be enrolled, including 5 patients with heart failure with preserved ejection fraction (HFpEF) and 5 patients with heart failure with reduced ejection fraction (HFrEF). The diagnosis of HFpEF and HFrEF will be based on the most recent European Society of Cardiology guidelines for the diagnosis and treatment of heart failure.~After their baseline blood sample collections, all participants will receive once-weekly subcutaneous semaglutide (Ozempyc, Novo Nordisk A/S Bagsvaerd, Denmark) at a dose of 0.25 mg for 2 weeks, 0.5 mg for 2 weeks, and then 1.0 mg for a period of 12 weeks. At the end of the 3-month and 4-month period, blood sample collections will be repeated. All blood samples will be sent to Stanford Cardiovascular Institute for further analyses. At baseline, and again at 4 months transthoracic echocardiography, 6-minute walk test, and body composition assessment will be performed."
RECRUITING
University Medical Center Ljubljana, Ljubljana
RECRUITING
Greenstone Biosciences, Palo Alto
RECRUITING
Stanford Cardiovascular Institute, Stanford
Collaborators (1)
Stanford University
OTHER
Greenstone Biosciences
UNKNOWN
University Medical Centre Ljubljana
OTHER