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Vitamin D and Its Affect on Growth Rates and Bone Mineral Density Until Age 5 (VitD)

Primary Purpose

Vitamin D Deficiency

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Vitamin D
Placebo (for Vitamin D)
Sponsored by
Meir Medical Center
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, Bone densitometry, Vitamin D supplementation, Growth

Eligibility Criteria

9 Months - 15 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Infants between 9-12 months old in Tipat Chalav and Kupat Holim Clalit in Beitar Illit undergoing a blood draw for CBC at one year of age.

Exclusion Criteria:

Parents that refuse to participate in this study, infants with any diagnosed chronic disease, and preterm infants less than 34 weeks.

Sites / Locations

  • Clalit Health services

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Placebo Comparator

No Intervention

Arm Label

Vit D supplementation

Placebo group

Normal group

Arm Description

Group 2-Infants with 25(OH)D below 15ng/ml receiving continued vitamin D supplementation of 800IU (4gtt/d) for one year.

Group 3- Infants with 25(OH)D below 15ng/ml those receiving the placebo.

Group 1- infants with 25(OH)D above 15ng/ml (normal levels) will receive no intervention.

Outcomes

Primary Outcome Measures

Height at the age of 3 years

Secondary Outcome Measures

Bone densitometry by ultrasound

Full Information

First Posted
August 17, 2011
Last Updated
February 21, 2013
Sponsor
Meir Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01419821
Brief Title
Vitamin D and Its Affect on Growth Rates and Bone Mineral Density Until Age 5
Acronym
VitD
Official Title
Supplemental Vitamin D Administered to One Year Old Vitamin D Deficient Infants Until Age 3 and Its Affect on Growth Rates and Bone Mineral Density Until Age 5
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Unknown status
Study Start Date
September 2013 (undefined)
Primary Completion Date
September 2014 (Anticipated)
Study Completion Date
September 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Meir Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Abstract Background: Vitamin D affects a wide variety of functions in the body including regulation of calcium, phosphorus, and bone metabolism. Israeli studies have documented a high prevalence of Vitamin D deficiency in Israeli infants in general, which was more severe in infants from Ultra-Orthodox Jewish families. Modest dress requirements in this population drastically reduce sun exposure, known to encourage production of Vitamin D. Countless research has analyzed preterm as well as term neonates born to mothers with vitamin D deficiency, with regard to weight, height, and bone mineral density at birth. However, there is a paucity of information about healthy infants' vitamin D levels and its' correlation to these parameters during the first few years of life. Objectives: The purpose of the proposed study is to measure and correlate levels of 25(OH)D and bone mineral density towards the end of the first year of life with growth rates and bone mineral density in the same children at the ages of 2, 3 and 5 years. Patients and Methods: The study will be performed in the Ultra-Orthodox Jewish community of Beitar Illit. 25(OH)D levels will be taken between 9-12 months of age (when routine blood tests are normally drawn for these infants) and bone mineral density will be measured using Quantitative Ultrasound. Infants will be divided into 2 groups: those with those with normal 25(OH)D levels (>15ng/ml), and those with 25(OH)D deficiency (<15ng/ml). Group 1- normal levels will receive no intervention. Infants with 25(OH)D below 15ng/ml will be randomly assigned into one of two groups; Group 2-those receiving continued vitamin D supplementation of 800 international units(IU) (4gtt/d) for one year, or Group 3- those receiving the placebo. Height, weight, and head circumference growth curves will be recorded every two months until 2 years of age. Quantitative ultrasound, growth charts and blood tests including 25(OH)D, serum calcium and phosphate levels, Parathyroid hormone (PTH), and alkaline phosphatase, taken at approximately 9-12 months will be repeated at 2 years of age. At that time children from Group 1 (no supplementation) will be divided into three: Group 1a- normal 25(OH)D levels will continue with no intervention, Group 1b <15ng/ml will begin receiving vitamin D 4gtt/d, Group 1c <15ng/ml will receive a placebo until age three. Groups 2 and 3 will continue their previous treatment until age three. All aforementioned tests will be repeated at age 3, when treatment will stop, and the same tests will be repeated at age 5.

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, Bone densitometry, Vitamin D supplementation, Growth

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vit D supplementation
Arm Type
Active Comparator
Arm Description
Group 2-Infants with 25(OH)D below 15ng/ml receiving continued vitamin D supplementation of 800IU (4gtt/d) for one year.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Group 3- Infants with 25(OH)D below 15ng/ml those receiving the placebo.
Arm Title
Normal group
Arm Type
No Intervention
Arm Description
Group 1- infants with 25(OH)D above 15ng/ml (normal levels) will receive no intervention.
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Other Intervention Name(s)
TipTipot Vitamin D 200IU/gtt
Intervention Description
800IU (4gtt/d) once a day for 2 years once a day.
Intervention Type
Other
Intervention Name(s)
Placebo (for Vitamin D)
Intervention Description
4gtt/d for the placebo for two years.
Primary Outcome Measure Information:
Title
Height at the age of 3 years
Time Frame
3 years after the recruitment begins
Secondary Outcome Measure Information:
Title
Bone densitometry by ultrasound
Time Frame
3 years after recruitment begins

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Months
Maximum Age & Unit of Time
15 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants between 9-12 months old in Tipat Chalav and Kupat Holim Clalit in Beitar Illit undergoing a blood draw for CBC at one year of age. Exclusion Criteria: Parents that refuse to participate in this study, infants with any diagnosed chronic disease, and preterm infants less than 34 weeks.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Avigdor Hevroni, MD
Phone
972508573982
Email
Avigdor@hadassah.org.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Avigdor Hevroni, MD
Organizational Affiliation
Hadassah Medical Organization
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clalit Health services
City
Beitar Elit
Country
Israel
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clalit
Phone
972-2-588-7000

12. IPD Sharing Statement

Citations:
PubMed Identifier
15585801
Citation
Greer FR. Issues in establishing vitamin D recommendations for infants and children. Am J Clin Nutr. 2004 Dec;80(6 Suppl):1759S-62S. doi: 10.1093/ajcn/80.6.1759S.
Results Reference
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Vitamin D and Its Affect on Growth Rates and Bone Mineral Density Until Age 5

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