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Clinical Trial Summary

Epicardial Fat (EAT), the visceral fat depot of the heart, is a modifiable cardio-metabolic risk factor and therapeutic target. EAT expresses GLP-1 receptors (GLP-1R). GLP-1 receptor agonist liraglutide is known to significantly decrease EAT thickness. However, the effects of GLP-1 receptor agonists semaglutide and dulaglutide on EAT thickness are unknown


Clinical Trial Description

This is a retrospective, observational, case control study. Data were obtained from retrospective review of the electronic medical records. Patients were treated with either semaglutide, dulaglutide or metformin as standard of care, during routine clinical practice, regardless of the study. Each patient underwent routine labs and an onsite ultrasound measurement of EAT thickness at baseline and at the routine 12-week follow up visit, as standard of care. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04200625
Study type Observational
Source University of Miami
Contact
Status Completed
Phase
Start date September 24, 2019
Completion date December 9, 2019

See also
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Not yet recruiting NCT01344694 - Epicardial Fat, Visceral Fat and Coronary Atherosclerosis N/A