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Prevention of Vitamin D Deficiency

Primary Purpose

Vitamin D Deficiency

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Vitamin D drops, 200 or 400 or 600 IU/day or 800 IU/day
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vitamin D Deficiency focused on measuring vitamin D deficiency, breastfed infant, northern latitude, infant, breastfed, winter, vitamin D status

Eligibility Criteria

3 Weeks - 5 Weeks (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Term infant
  • No major congenital malformations
  • Less than one month old
  • Breastfed, no other foods

Exclusion Criteria:

  • Formula feeding
  • Premature birth

Sites / Locations

  • MTF, 2501 Crosspark Rd

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

200 IU/day Vitamin D

400 IU/day Vitamin D

600 IU/day Vitamin D

800 IU/day Vitamin D

Arm Description

200 IU/day Vitamin D

400 IU/day Vitamin D

600 IU/day Vitamin D

800 IU/day Vitamin D

Outcomes

Primary Outcome Measures

Plasma concentrations of 25-hydroxyvitamin D, parathyroid hormone, alkaline phosphatase

Secondary Outcome Measures

whole body mineral content by DEXA

Full Information

First Posted
June 28, 2007
Last Updated
December 14, 2012
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00494104
Brief Title
Prevention of Vitamin D Deficiency
Official Title
Prevention of Vitamin D Deficiency in Breastfed Infants
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Breastfed infants living in a northern location (41 degrees N) are at high risk of vitamin D deficiency during winter. This trial is designed to determine how much supplemental vitamin D breastfed infants need to receive in order to remain free of vitamin D deficiency
Detailed Description
It is increasingly being recognized that infants and children living at northern latitudes are at risk of vitamin D deficiency, especially if their skin is darkly pigmented. The study by the PI (Pediatrics 2006;118:603) was the first to demonstrate that infants with light skin pigmentation living at 41 degrees north are at risk of vitamin D deficiency. During winter (December - April) a full 78% of infants were vitamin D deficient if they did not receive vitamin D from an external source. Very few breastfed babies are currently receiving supplemental vitamin D. The recommended dose is 200 IU/day. However, there are questions about the adequacy of this dose of vitamin D for the prevention of vitamin D deficiency. The present trial is designed to determine whether a dose of 200 IU/day is effective or whether doses of 400 IU/day, 600 IU/day or 800 IU/day are required to prevent vitamin D deficiency reliably. The trial is a randomized, prospective double-blind trial in which breastfed infants will receive 200 IU/day or 400 IU/day or 600 IU/day or 800 IU/day from 1 to 9 months of age. There will not be a placebo control group. Infants will be followed through 12 months of age. Normal term infants (birth weight >2500 g) who are born in June through November will be enrolled and randomized at 1 month of age. They will visit the study center at monthly intervals and will have capillary blood drawn at select ages. At 2 months and again in March or April whole body mineral content will be determined by DEXA. Infants will not be permitted to receive formula until 9 months of age. They may receive complementary foods beginning at 4 months of age. Vitamin D supplements will be weighed before dispensing and again when the empty and half-empty containers are returned. Study endpoints will be blood parameters and bone mineral content determined at the end of winter, i.e., between March and May 15. Blood parameters include 25-OHD, parathyroid hormone, calcium, alkaline phosphatase, osteocalcin, N-telopeptide, ferritin and transferrin receptor. 180 infants will be enrolled at 1 month of age in the expectation that 48 per group will complete the trial to at least 9 months of age.

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 deficiency, breastfed infant, northern latitude, infant, breastfed, winter, vitamin D status

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
398 (Actual)

8. Arms, Groups, and Interventions

Arm Title
200 IU/day Vitamin D
Arm Type
Active Comparator
Arm Description
200 IU/day Vitamin D
Arm Title
400 IU/day Vitamin D
Arm Type
Experimental
Arm Description
400 IU/day Vitamin D
Arm Title
600 IU/day Vitamin D
Arm Type
Experimental
Arm Description
600 IU/day Vitamin D
Arm Title
800 IU/day Vitamin D
Arm Type
Experimental
Arm Description
800 IU/day Vitamin D
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D drops, 200 or 400 or 600 IU/day or 800 IU/day
Intervention Description
Infants receive daily 0.5 ml of code labeled supplement
Primary Outcome Measure Information:
Title
Plasma concentrations of 25-hydroxyvitamin D, parathyroid hormone, alkaline phosphatase
Time Frame
end of winter
Secondary Outcome Measure Information:
Title
whole body mineral content by DEXA
Time Frame
end of winter

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Weeks
Maximum Age & Unit of Time
5 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Term infant No major congenital malformations Less than one month old Breastfed, no other foods Exclusion Criteria: Formula feeding Premature birth
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ekhard Ziegler, MD
Organizational Affiliation
University of Iowa
Official's Role
Principal Investigator
Facility Information:
Facility Name
MTF, 2501 Crosspark Rd
City
Coralville
State/Province
Iowa
ZIP/Postal Code
52241-8802
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24858141
Citation
Ziegler EE, Nelson SE, Jeter JM. Vitamin D supplementation of breastfed infants: a randomized dose-response trial. Pediatr Res. 2014 Aug;76(2):177-83. doi: 10.1038/pr.2014.76. Epub 2014 May 23.
Results Reference
derived

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Prevention of Vitamin D Deficiency

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