Vitamin D Deficiency in Adults Following a Major Burn Injury

Status Recruiting

Clinical Trial Summary

This is a single site double blind randomized controlled trial of replacing Vitamin D for Vitamin D-deficient burn patients at a current recommended dose (400 IU daily) versus a higher dose (4000 IU daily). Capsules will be made in a compounding pharmacy and will look identical. Randomized controlled trial. People who meet the selection criteria will be randomized to either low or high dosage of Vitamin D. Treatment arm is high dose Vitamin D (4000 IU), and control is low dose Vitamin D (400 IU). Main outcome variables include PROMIS-29 measures of physical health, mental health and social health, the Veterans RAND 12 Item Health Survey (VR-12), and the 4-D Itch Scale. Secondary outcome variables include subject demographics, injury demographics and characteristics.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05084248
Study type	Interventional
Source	University of Texas Southwestern Medical Center
Contact	Kyra Jeanine Solis, BS
Phone	214-648-3560
Email	KyraJeanine.Solis@UTSouthwestern.edu
Status	Recruiting
Phase	Phase 4
Start date	September 29, 2022
Completion date	March 2025

View Details

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