Obesity Clinical Trial
Official title:
Evaluating Hormonal Mechanisms for Vitamin D Receptor Agonist Therapy in Diabetes: The VALIDATE-D Study
The purpose of this study is to evaluate whether vitamin D receptor agonist therapy lowers renin-angiotensin system activity.
This study aims to evaluate whether vitamin D receptor agonist therapy (calcitriol) in
diabetes lowers renin-angiotensin system (RAS) activity in a manner similar to an ACE
inhibitor. This is a physiology study, focused on evaluating hormonal changes in the
circulating and tissue RAS when compared to placebo.
Subjects with type 2 diabetes and obesity and normal kidney function will undergo evaluation
of their circulating and renal-vascular RAS activity and urinary protein at baseline, after
withdrawing interfering medications, while on a controlled electrolyte diet, and in
controlled posture settings. They will then randomly receive a study medication (calcitriol
or placebo) for 3 weeks followed by a re-assessment of their RAS parameters. The main
outcomes that will be evaluated following calcitriol/placebo include measures of the
circulating RAS (primary), as well as measures of the renal-vascular RAS, urine protein,
adipocytokine levels, and adipose-tissue RAS activity (secondary)
In an extension phase, Lisinopril will be added to the study drug for another 2 weeks
followed by another assessment of the primary and secondary outcome parameters, and subjects
will continue lisinopril+study drug for 3 additional months for one final assessment of RAS
parameters and urinary protein.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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