search
Back to results

Vitamin D Deficiency in Adults Following a Major Burn Injury

Primary Purpose

Vitamin D Deficiency, Burns

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ergocalciferol Capsules
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Deficiency

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Adults, 18 years of age or older, who have completed 6 months from time of their burn injury
  2. ≥ 10% TBSA, ≥ 65 years of age and Burn Surgery for Wound Closure
  3. ≥ 20% TBSA, 18 - 64 of age and Burn Surgery for Wound Closure
  4. Electrical high voltage / lightning and Burn Surgery for Wound Closure
  5. Hand burn and/or face burn, and/or feet burn and Burn Surgery for Wound Closure
  6. May speak English or Spanish
  7. Vit. D deficiency

Exclusion Criteria:

  1. Patients with parathyroid disease, severe liver dysfunction, sever kidney dysfunction, which are not caused by the burn injury
  2. Patients with malignant tumors
  3. Patients not meeting the inclusion criteria

Sites / Locations

  • Parkland Health and Hospital SystemsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Low-dose

High-dose

Arm Description

400 IU Per Orem

4000 IU Per Orem

Outcomes

Primary Outcome Measures

Patient-Reported Outcomes Measurement Information System-29
Measures change in physical health, mental health and social health between time points. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores on anxiety indicate more anxiety, while higher scores on physical function indicate higher physical function. Please see more information here: https://www.healthmeasures.net/explore-measurement-systems/promis/intro-to-promis.

Secondary Outcome Measures

Demographics
include subject demographics, injury demographics and characteristics
Patient-Reported Outcomes Measurement Information System-Global
Measures change in emotional, physical, and social health between timepoints. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores indicates a higher global health.
Patient-Reported Outcomes Measurement Information System-Itch
Measures change in itch between timepoints. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores indicate more itch.

Full Information

First Posted
September 27, 2021
Last Updated
October 9, 2023
Sponsor
University of Texas Southwestern Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT05084248
Brief Title
Vitamin D Deficiency in Adults Following a Major Burn Injury
Official Title
Vitamin D Deficiency in Adults Following a Major Burn Injury
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 29, 2022 (Actual)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency, Burns

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low-dose
Arm Type
Active Comparator
Arm Description
400 IU Per Orem
Arm Title
High-dose
Arm Type
Experimental
Arm Description
4000 IU Per Orem
Intervention Type
Drug
Intervention Name(s)
Ergocalciferol Capsules
Other Intervention Name(s)
Vitamin D
Intervention Description
Capsules of ergocalciferol at 400 IU and 4000 IU
Primary Outcome Measure Information:
Title
Patient-Reported Outcomes Measurement Information System-29
Description
Measures change in physical health, mental health and social health between time points. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores on anxiety indicate more anxiety, while higher scores on physical function indicate higher physical function. Please see more information here: https://www.healthmeasures.net/explore-measurement-systems/promis/intro-to-promis.
Time Frame
6 months and 12 months
Secondary Outcome Measure Information:
Title
Demographics
Description
include subject demographics, injury demographics and characteristics
Time Frame
6 months
Title
Patient-Reported Outcomes Measurement Information System-Global
Description
Measures change in emotional, physical, and social health between timepoints. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores indicates a higher global health.
Time Frame
6 months and 12 months
Title
Patient-Reported Outcomes Measurement Information System-Itch
Description
Measures change in itch between timepoints. When the scores are transformed into t-score metric, all PROMIS measures range from 0-100. For each domain, the higher scores indicate more of what is being measured. Therefore, higher scores indicate more itch.
Time Frame
6 months and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults, 18 years of age or older, who have completed 6 months from time of their burn injury ≥ 10% TBSA, ≥ 65 years of age and Burn Surgery for Wound Closure ≥ 20% TBSA, 18 - 64 of age and Burn Surgery for Wound Closure Electrical high voltage / lightning and Burn Surgery for Wound Closure Hand burn and/or face burn, and/or feet burn and Burn Surgery for Wound Closure May speak English or Spanish Vit. D deficiency Exclusion Criteria: Patients with parathyroid disease, severe liver dysfunction, sever kidney dysfunction, which are not caused by the burn injury Patients with malignant tumors Patients not meeting the inclusion criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kyra Jeanine Solis, BS
Phone
214-648-3560
Email
KyraJeanine.Solis@UTSouthwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Karen Kowalske, MD
Phone
214-645-2080
Email
karen.kowalske@utsouthwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Pia Kabamalan
Organizational Affiliation
UT Southwestern
Official's Role
Study Chair
Facility Information:
Facility Name
Parkland Health and Hospital Systems
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kyra Jeanine Solis, BS
Phone
214-648-3560
Email
KyraJeanine.Solis@UTSouthwestern.edu
First Name & Middle Initial & Last Name & Degree
Karen Kowalske, MD
Phone
214-645-2080
Email
Karen.Kowalske@UTSouthwestern.edu

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data may be shared with Burn Model System under National Institute on Disability and Rehabilitation Research.

Learn more about this trial

Vitamin D Deficiency in Adults Following a Major Burn Injury

We'll reach out to this number within 24 hrs