MedPath

Early Infant Micronutrition and Development

Phase 2
Recruiting
Conditions
Vitamin B 12 Deficiency
Interventions
Biological: Cyanocobalamin
Registration Number
NCT05005897
Lead Sponsor
Sykehuset Innlandet HF
Brief Summary

Globally, vitamin B12 deficiency is one of the most common micronutrient deficiencies. Poor status is also seen in affluent countries such as in Norway. Vitamin B12 is crucial for normal cell division and differentiation and necessary for the development and myelination of the central nervous system. Deficiency is also associated with impaired fetal and infant growth. In the proposed study we will measure the effect of daily oral vitamin B12 supplementation infants on neurodevelopment. We also aim to measure the impact of B12 supplementation on several other outcomes.

Study design: Individually randomized double-blind placebo-controlled trial breastfed infants who will be assigned to a screening group (in which measurements will be obtained immediately) or a control group (in which serum will be stored and measurements done after one year).

Pregnant women will be informed about the study during their first antenatal visit at the clinic and that we will re-approach them on their 6-week visit to their public health nurse. Infants who are deficient will be treated with peroral or intramuscular injections with 400 µg cyano-cobalamin.

Infants in the control group will not be offered any intervention their blood sample will be stored for one year and then analyzed for the same nutrients as the intervention group.

Outcomes: Primary: (i) neurodevelopment in children measured at 12 months of age (ii) growth in children measured by attained weight and length at 12 months. Secondary: (i) neurodevelopment and cognitive functioning in children later in life

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
600
Inclusion Criteria
  1. Availability of informed verbal consent
  2. Plan to reside in the defined study area for the next 12 months
  3. Mothers intend to breastfeed their children for at least 8 months, and exclusively for 4 months
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Exclusion Criteria
  1. Severe systemic illness requiring hospitalization
  2. Growth retardation
  3. Severe congenital malformations
  4. Plasma cobalamin concentration <148 pmol/L (These children will be treated for vitamin B12 deficiency and not included in the RCT, but will be included in the cohort design)
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Screening - treatmentCyanocobalaminFrom 6 weeks of age, infants will be screened for elevated plasma total homocysteine concentrations. Those who have a concentration above the defined cut-off will be treated with cobalamin (vitamin B12).
Primary Outcome Measures
NameTimeMethod
Prevalence of vitamin B12 deficiency1-3 months of age

Number of children with elevated plasma homocysteine or low cobalamin

Prevalence of other vitamin deficiencies1-3 months of age

Number of infants with vitamin deficiencies other than vitamin B12 deficiency

Neurodevelopment12 months of age

Bayley Scales of Infant Development 4th edition

Secondary Outcome Measures
NameTimeMethod
Neurodevelopment measured by the Ages and Stages Questionaire4-12 months of age

Ages and Stages Questionnaire version 3 repeated throughout infancy

Vagal tone12 months of age

Heart rate variability

Eye tracking12 months of age

Visual acuity, visuospatial orientation, and attention to social cues

Neurodevelopment later in childhood5 years

General cognitive abilities ("IQ") assessed by the Wechsler Preschool and Primary Scale of Intelligence

Adverse events3 months after treatment with vitamin B12

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

Trial Locations

Locations (1)

Innlandet Hospital Trust

🇳🇴

Lillehammer, Norway

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