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Clinical Trial Summary

This study evaluates whether achieving 25-hydroxyvitamin D (25[OH] Vit D) levels (>40 ng/mL) among myocardial infarction patients will result in a reduction of cardiovascular-related adverse events. Half of the patients will be randomized to receive standard of care and half will receive clinical management of 25[OH] Vit D levels.


Clinical Trial Description

Low 25[OH] Vit D levels have become a public epidemic with increasing recognition of its widespread insufficiency both in the United States and worldwide. Epidemiologic studies have associated low 25[OH] Vit D levels with coronary risk factors and adverse cardiovascular outcomes. However, randomized trials are needed to establish the relevance of 25[OH] Vit D status to cardiovascular health. While a few randomized trials have evaluated vitamin D supplementation, none have "treated to target" (i.e., individual dosing so that adequate 25[OH] Vit D levels are obtained), but have rather given "blanket" doses regardless of 25[OH] Vit D level. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02996721
Study type Interventional
Source Intermountain Health Care, Inc.
Contact Heidi T May, PhD, MSPH
Phone 801-507-4822
Email [email protected]
Status Recruiting
Phase Phase 4
Start date April 3, 2017
Completion date April 2023

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