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Effect of Oral Daily Supplementation With 400 IU Vs 200 IU of Vitamin D in Term Healthy Neonates

Primary Purpose

Vitamin D Deficiency

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Vitamin D
Sponsored by
Lady Hardinge Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vitamin D Deficiency focused on measuring oral daily supplementation with vitamin D for 6 months

Eligibility Criteria

2 Hours - 48 Hours (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Gestation > 37 weeks
  • Birth weight >2.5 kg
  • Informed consent of one of the parents
  • Place of residence<10km

Exclusion Criteria:

  • Presence of gross congenital malformation
  • Need of resuscitation at birth
  • Need for admission to neonatal ICU
  • Refusal of consent

Sites / Locations

  • Kalawati Saran children's Hospital, Lady Hardinge Medical College

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Vitamin D 400 IU

Vitamin D 200IU

Arm Description

Vitamin D-400IU/ml- 1ml daily Neonates will be administered Vitamin D 400 IU orally daily by the mother or other caregiver for a period of six months. The neonates will be followed up for compliance at 2 weeks, 6, 10 and 14 weeks and thereafter at 6 months of age.

Vitamin D 400IU/ml : 0.5ml daily Neonates will be administered Vitamin D 200 IU orally daily by the mother or other caregiver for a period of six months. The neonates will be followed up for compliance at 2 weeks, 6, 10 and 14 weeks and thereafter at 6 months of age.

Outcomes

Primary Outcome Measures

Difference in vitamin D levels attained after oral supplementation with 400IU/day Vs 200IU/day of vitamin D for 6 months

Secondary Outcome Measures

Proportion of vitamin D deficient term healthy neonates at birth
serum vitaminD levels > 20 ng/ml - sufficient 15 - 20 ng/ml - insufficient <15 ng/ml - deficient

Full Information

First Posted
July 7, 2014
Last Updated
September 26, 2015
Sponsor
Lady Hardinge Medical College
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1. Study Identification

Unique Protocol Identification Number
NCT02186028
Brief Title
Effect of Oral Daily Supplementation With 400 IU Vs 200 IU of Vitamin D in Term Healthy Neonates
Official Title
Effect Of Oral Daily Supplementation With 400 IU Vs 200 IU Of Vitamin D In Term Healthy Newborns: A Randomised Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lady Hardinge Medical College

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to evaluate the effect of daily oral supplementation with vitamin D on serum Vitamin D levels in term healthy newborns. It has been found in various studies that vitamin D is highly deficient in Indian mother infant diads. There is a need to supplement vitamin D from neonatal period to prevent various metabolic disturbances due to vitamin D deficiency in later life. This study aims to find the effectiveness and the optimum dose of routine vitamin D supplementation in healthy term newborns for fulfilling the normal requirements in Indian infants.
Detailed Description
Vitamin D deficiency is highly prevalent in India as reported in various studies. Vitamin D supplementation is necessary as vitamin D is required not only for prevention of rickets as traditionally thought, but also for its emerging role in development of diseases such as myopathic disorders, proneness to infection, autoimmune disorders and cancers .However supplementation studies are limited and predominantly from foreign countries. Moreover most of them report variable outcomes with no unanimous outcome with respect to optimum dose and duration of supplementation of vitamin D. Various national authorities recommend different doses of vitamin D for supplementation. American Academy of Pediatrics, The Institute of Medicine of National Academics, The Drug and Therapeutics Committee of the Lawson Wilkins Pediatric Endocrine Society, the Canadian Pediatric Society and European Society for Pediatric Endocrinology recommend that 400IU of vitamin D should be supplemented in all infants starting from within a few days of birth throughout childhood. ESPGHAN recommends 800-1000 IU for high risk infants, Ireland recommends 200IU vitamin D per day, UK does not recommend any supplements upto 6 months of age , however if formula milk intake <500ml/day then 300 IU is recommended. There are no such guidelines for India. Hence this study aims at evaluating the proportion of vitamin D deficient

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency
Keywords
oral daily supplementation with vitamin D for 6 months

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D 400 IU
Arm Type
Experimental
Arm Description
Vitamin D-400IU/ml- 1ml daily Neonates will be administered Vitamin D 400 IU orally daily by the mother or other caregiver for a period of six months. The neonates will be followed up for compliance at 2 weeks, 6, 10 and 14 weeks and thereafter at 6 months of age.
Arm Title
Vitamin D 200IU
Arm Type
Active Comparator
Arm Description
Vitamin D 400IU/ml : 0.5ml daily Neonates will be administered Vitamin D 200 IU orally daily by the mother or other caregiver for a period of six months. The neonates will be followed up for compliance at 2 weeks, 6, 10 and 14 weeks and thereafter at 6 months of age.
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Intervention Description
Vit D 400 IU vs. Vit D 200 IU
Primary Outcome Measure Information:
Title
Difference in vitamin D levels attained after oral supplementation with 400IU/day Vs 200IU/day of vitamin D for 6 months
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Proportion of vitamin D deficient term healthy neonates at birth
Description
serum vitaminD levels > 20 ng/ml - sufficient 15 - 20 ng/ml - insufficient <15 ng/ml - deficient
Time Frame
at birth
Other Pre-specified Outcome Measures:
Title
Proportion of neonates having vitamin D sufficiency after supplementation
Description
serum vitamin D levels > 20 ng/ml - sufficient 15 - 20 ng/ml - insufficient <15 ng/ml - deficient
Time Frame
6 months
Title
Proportion of neonates having vitamin D deficiency after supplementation
Description
serum vitamin D levels > 20 ng/ml - sufficient 15 - 20 ng/ml - insufficient <15 ng/ml - deficient
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Hours
Maximum Age & Unit of Time
48 Hours
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Gestation > 37 weeks Birth weight >2.5 kg Informed consent of one of the parents Place of residence<10km Exclusion Criteria: Presence of gross congenital malformation Need of resuscitation at birth Need for admission to neonatal ICU Refusal of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sushma Nangia, MD, DM
Organizational Affiliation
Lady Hardinge Medical College & Kalawati Saran Children's Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Arvind Saili, MD
Organizational Affiliation
Lady Hardinge Medical College & Kalawati Saran Children's Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Kalawati Saran children's Hospital, Lady Hardinge Medical College
City
New Delhi
ZIP/Postal Code
110001
Country
India

12. IPD Sharing Statement

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Effect of Oral Daily Supplementation With 400 IU Vs 200 IU of Vitamin D in Term Healthy Neonates

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