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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Postprandial Fatty Acid Metabolism in Subjects With Lipoprotein Lipase DeficiencyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, familial lipoprotein lipase deficiency, hereditary disease, hyperlipidemia, hyperlipoproteinemia, inborn errors of metabolism, metabolic diseaseRecruitingNot applicable2026-02-10NCT04227678

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Research sitesCityCountryLinked trials
Centre de Recherche du CHUSSherbrookeCanada9