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The Pharmacokinetics of a Single Large Dose of Vitamin D3 (Stoss)

Primary Purpose

Vitamin D Deficiency

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
cholecalciferol.
Sponsored by
Creighton University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Deficiency focused on measuring vitamin D, cholecalciferol, 25-hydroxyvitamin D

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • healthy with limited sun exposure of less than 10 hours per week and daily milk consumption of less than 0.47 L (16 oz.).

Exclusion Criteria:

  • those with granulomatous conditions, liver disease, kidney disease, or diabetes and those taking anticonvulsants, barbiturates, or steroids in any form.

Sites / Locations

  • Creighton University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

cholecalciferol

Control

Arm Description

A single dose of 100,000 IU vitamin D

No drug was given

Outcomes

Primary Outcome Measures

to assess the time course and response of serum 25-OHD with a single oral dose of 100,000 IU cholecalciferol.

Secondary Outcome Measures

Full Information

First Posted
May 11, 2007
Last Updated
April 30, 2015
Sponsor
Creighton University
Collaborators
Procter and Gamble
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1. Study Identification

Unique Protocol Identification Number
NCT00473239
Brief Title
The Pharmacokinetics of a Single Large Dose of Vitamin D3
Acronym
Stoss
Official Title
The Pharmacokinetics of a Single Large Dose of Vitamin D3
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
October 2006 (undefined)
Primary Completion Date
March 2007 (Actual)
Study Completion Date
March 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Creighton University
Collaborators
Procter and Gamble

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
When people eat a meal, some, but not all of the calcium in that meal is absorbed, that is, moved into the bloodstream. When the skin is exposed to sunlight during summer months, Vitamin D is made there and then modified into more active forms by the liver and kidneys. These more active forms of Vitamin D improve calcium absorption. Many adults living in the U.S. have little or no sun exposure and are low in Vitamin D. A single dose of 100,000 IU of Vitamin D3 has been used both as empiric treatment for Vitamin D deficiency as well as in controlled trials without risk of raising blood calcium to dangerous levels.This study is to determine the serum levels of Vitamin D and 25-hydroxyvitamin D (vitamin D after it has been modified by the liver) that can be expected when Vitamin D3 is given as a single oral dose of 100,000 IU.
Detailed Description
The group receiving the supplement will be scheduled for short visits to our research center at baseline and days 1,3,5,7 and then weekly for 3 weeks and then every other week for 6 visits (total 14 visits in 4 months). The group not receiving supplement will be scheduled for short visits at baseline and in 4 months. At the beginning of the study we will measure your height, weight, skin color, and draw blood to measure your blood levels of Vitamin D, 25-hydroxyvitamin D, calcium and parathyroid hormone. At each visit we will draw blood to measure your blood levels of Vitamin D and 25-hydroxyvitamin D. There will be fourteen blood draws for a total of 280 cc of blood drawn (about 4 teaspoons drawn each time) in the supplemented group. There will be 2 blood draws in the group not receiving supplements for a total of 60 cc of blood drawn (about 4 teaspoons drawn each time).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency
Keywords
vitamin D, cholecalciferol, 25-hydroxyvitamin D

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
cholecalciferol
Arm Type
Experimental
Arm Description
A single dose of 100,000 IU vitamin D
Arm Title
Control
Arm Type
No Intervention
Arm Description
No drug was given
Intervention Type
Drug
Intervention Name(s)
cholecalciferol.
Other Intervention Name(s)
vitamin D
Intervention Description
100,000 IU of Vitamin D
Primary Outcome Measure Information:
Title
to assess the time course and response of serum 25-OHD with a single oral dose of 100,000 IU cholecalciferol.
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy with limited sun exposure of less than 10 hours per week and daily milk consumption of less than 0.47 L (16 oz.). Exclusion Criteria: those with granulomatous conditions, liver disease, kidney disease, or diabetes and those taking anticonvulsants, barbiturates, or steroids in any form.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laura A Armas, MD
Organizational Affiliation
Creighton University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Creighton University
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68131
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18326608
Citation
Ilahi M, Armas LA, Heaney RP. Pharmacokinetics of a single, large dose of cholecalciferol. Am J Clin Nutr. 2008 Mar;87(3):688-91. doi: 10.1093/ajcn/87.3.688.
Results Reference
derived

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The Pharmacokinetics of a Single Large Dose of Vitamin D3

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