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Vitamin A Supplementation at Birth and Atopy in Childhood

The Effect of Vitamin A Supplementation at Birth on the Development of Atopy in Childhood: Long-term Follow-up of a Randomised Placebo-controlled Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01779180
Enrollment
2000
Registered
2013-01-30
Start date
2013-01-31
Completion date
2014-02-28
Last updated
2013-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, Atopy, Eczema, Food Allergy

Keywords

Vitamin A supplementation, BCG vaccination, diphtheria-tetanus-pertussis vaccination, measles vaccination, atopy

Brief summary

INTRODUCTION Eight trials studying the effect of providing neonatal vitamin A supplementation (NVAS) have been reported, and another four are underway to test whether NVAS should become WHO policy. Three of the four African trials were conducted by the Bandim Health Project (BHP) in Guinea-Bissau. One of them was a two-by-two factorial trial among low-birth-weight children. From 2004-2008, the children were randomly allocated to 25,000 IU vitamin A or placebo at birth, and furthermore to BCG vaccination at birth or later as is local policy. In 2011, the investigators conducted a follow-up study. A remarkably strong harmful effect of NVAS on atopy and wheezing was found (manuscript under review). Seen in the context that NVAS may soon become a WHO policy it is obviously worrying if NVAS is associated with a higher risk of atopy and wheezing. The investigators therefore aim to conduct a similar follow-up study of participants in the first NVAS trial conducted in Guinea-Bissau from 2002-2004, among normal-birth-weight infants, to test whether NVAS is associated with an increased risk of atopy and wheezing and other allergic symptoms as well as growth. METHODS Study population: From 2002-2004 BHP conducted a randomised trial of NVAS. The investigators recruited newborns when they came for BCG vaccination. Provided parental consent, they received an oral supplement of 50,000 IU vitamin A or placebo. Study design: This study will be a follow-up study of the cohort of children randomised to NVAS (intervention) or placebo (current policy) together with BCG vaccine at birth. Other exposures: The investigators will also investigate the effect of receiving an additional dose of measles vaccine and the timing of DTP vaccine on the development of atopy. Assessment of outcomes: The investigators will visit all children at the last known address. Height, weight and mid upper arm circumference will be measured. BCG scar will be examined and vaccination card details recorded by the field assistant. Children will be excluded from skin prick testing (SPT) if they have a history suggestive of anaphylaxis or are currently using anti-histamine medication. SPT will be performed using aero-allergens, food allergens and positive histamine and negative saline control. The mother or guardian will be interviewed by a local assistant. Symptoms of eczema and asthma as well as food allergy will be assessed. Statistical analysis: Effect of randomisation group and other factors on outcomes will be analysed in multivariable regression models. All analyses will be adjusted for skin prick tester. All analyses will be conducted stratified by sex.

Interventions

None listed

Sponsors

Bandim Health Project
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Enrolled at birth in NCT00168610

Exclusion criteria

* Children with history suggestive of anaphylaxis will be excluded from skin prick testing but included in the study population

Design outcomes

Primary

MeasureTime frameDescription
Atopic sensitisationSingle observation on day of recruitmentSkin prick test positivity. A wheal \>=3mm will be considered positive.

Secondary

MeasureTime frameDescription
Symptoms of asthmaSingle observation on day of recruitmentQuestionnaire based on ISAAC survey for 6-7 year olds
Symptoms of eczemaSingle observation on day of recruitmentQuestionnaire based on ISAAC survey for 6-7 year olds
Symptoms of food allergySingle observation of day of recruitmentQuestionnaire based on Health Nuts survey

Other

MeasureTime frameDescription
WeightSingle observation on day of recruitment
Infectious diseasesSingle observation on day of recruitmentHistory of chickenpox or measles
HeightSingle observation on day of recruitment
Mid-upper arm circumferenceSingle observation on day of recruitment
HospitalisationsSingle observation on day of recruitment

Countries

Guinea-Bissau

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026