High-Dose Vitamin D Deficiency in Burn Injury (VitaminD)
Primary Purpose
Burn
Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Vitamin D
Sponsored by
About this trial
This is an interventional treatment trial for Burn focused on measuring burn, vitamin D, nutrition, burn recovery
Eligibility Criteria
Inclusion Criteria:
- 5+ yrs
- Burn size 40% or greater
- Patient can remain around Shriner Hospital for Children area for 16 weeks
- Agree to take Vitamin D
Exclusion Criteria:
- Age less than 5yrs
- Burn size less than 40%
- Pre-existing bone disease or healing fractures
- Underlying chronic disease-endocrine or cancer
- Kidney failure
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
Vitamin D administration
Outcomes
Primary Outcome Measures
Increase in overall bone health
Secondary Outcome Measures
Full Information
NCT ID
NCT00591604
First Posted
December 26, 2007
Last Updated
November 13, 2012
Sponsor
The University of Texas Medical Branch, Galveston
1. Study Identification
Unique Protocol Identification Number
NCT00591604
Brief Title
High-Dose Vitamin D Deficiency in Burn Injury
Acronym
VitaminD
Official Title
Use of High-Dose Vitamin D to Treat Vitamin D Deficiency Following Severe Burn Injury in Children I: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
November 2012
Overall Recruitment Status
Withdrawn
Why Stopped
hurricane caused closure of hospital with PI not associated with Shriners Hospital for children
Study Start Date
February 2007 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
March 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Medical Branch, Galveston
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
High dose Vitamin D (50,000IU) therapy may increase bone mineral density/bone mineral content after large burns.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burn
Keywords
burn, vitamin D, nutrition, burn recovery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Vitamin D administration
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Intervention Description
Vitamin D, 50,000IU,once weekly for 8 weeks, then every other week for 4 weeks
Primary Outcome Measure Information:
Title
Increase in overall bone health
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
5+ yrs
Burn size 40% or greater
Patient can remain around Shriner Hospital for Children area for 16 weeks
Agree to take Vitamin D
Exclusion Criteria:
Age less than 5yrs
Burn size less than 40%
Pre-existing bone disease or healing fractures
Underlying chronic disease-endocrine or cancer
Kidney failure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David N Herndon, MD
Organizational Affiliation
University of Texas
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
High-Dose Vitamin D Deficiency in Burn Injury
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