Clinical Research Directory

Inclusion Criteria: * Male or female participants aged 18-60 years. * Participants with fasting triglyceride levels \<150 mg/dL (after fasting for at least 8-12 hours before blood collection). * Participants without a history of cardiovascular disease, diabetes mellitus, thyroid disease, cancer, liver disease, or kidney disease. * Participants who are able to read and write. * Participants who voluntarily agree to participate after receiving information regarding the study objectives, procedures, potential risks, and expected benefits; are able to comply with the study protocol; and provide written informed consent. Exclusion Criteria: * Participants with a history of allergy or adverse reactions, such as skin, respiratory, or gastrointestinal symptoms, after consuming foods containing canola oil, polyglycerol esters of fatty acids (PGEs), green tea extract, palm oil, or banana. * Participants who have consumed medications, dietary supplements, herbal products, or foods that may affect metabolism, such as weight-loss products or L-carnitine, within 2 weeks prior to enrollment. * Participants who regularly use medications that may affect lipid metabolism or blood lipid levels, such as corticosteroids or lipid-lowering agents. * Participants with serious underlying diseases or poorly controlled medical conditions, such as cancer, cardiovascular disease, or immunodeficiency disorders. * Participants with impaired liver or kidney function, defined as AST/ALT levels \>3 times the upper limit of normal or kidney disease with an estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73 m². * Female participants who are pregnant or breastfeeding. * Participants who regularly smoke. * Participants who regularly consume alcohol. * Participants who are currently participating in another research study.