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Iodine Supplementation During Pregnancy and Neuropsychological Development

Effect of Iodine Supplementation and During Pregnancy on Neuropsychological Development of Children Assessed at 2 Years Old

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01049659
Enrollment
85
Registered
2010-01-14
Start date
2010-02-01
Completion date
2011-06-01
Last updated
2026-03-31

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

Conditions

Healthy, Iodine Deficiency, Pregnancy

Keywords

pregnancy, iodine deficiency, neuropsychological development

Brief summary

The investigators have shown that Nice area, like most of France, remains an area of mild iodine deficiency. The investigators want to assess the potential benefit of early iodine supplementation during pregnancy in women with normal thyroid function on the neuropsychological development of their children assessed at the age of two with the Bayley test.

Detailed description

Iodine is required for the synthesis of thyroid hormones. During pregnancy, iodine needs are increased to cover maternal and fetal thyroid hormones synthesis and the increased renal iodine clearance. Maternal hypothyroidism and/or severe iodine deficiency are associated to mental retardation in their offspring. Indeed, thyroid hormones and iodine are necessary for fetal brain development. Iodine deficiency remains the first cause of preventable mental retardation. In France, preventive programs with salt iodine fortification are insufficient to eradicate iodine deficiency. In previous studies, we have shown that iodine deficiency is the rule for pregnant women in our area: 66 to 85% of women tested depending on the stage of pregnancy (Brucker-Davis 2004, Hieronimus et al 2009, abstract at the 2008 ETA and SFE meetings, article in preparation reporting results from our 2006 PHRC: Study of thyroid function during pregnancy with or without iodine supplementation).We will study the impact of early iodine supplementation in normal pregnant women on the neuropsychological development of their offspring assessed at 2 years of age. This is the follow-up of a cohort of children born to women enrolled in our 2006 PHRC. 110 healthy women have been included in this prospective study: they were seen early (median 8 weeks of gestation) and had strictly normal thyroid function tests, as well as no personal thyroid history. They were randomized into two groups: group A taking pregnancy vitamins without iodine supplementation (Oligobs GrossesseR 2 tablets/day) our group B taking the same vitamins but iodine fortified (Oligobs MaxiodeR 2 tablets per day, i.e. 150 mcg of iodine/day).

Interventions

Bayley test (version III) which provides several scales of development. Children are assessed just one time at two year old

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
23 Months to 25 Months
Healthy volunteers
Yes

Inclusion criteria

* children which mother were included in the precedent protocol(pregnancy vitamins with or without iodine)

Exclusion criteria

* children of more of 25 months old * children with acute pathology * children with chronic pathology

Design outcomes

Primary

MeasureTime frame
neuropsychological testone time mesure- just one visit in the study

Countries

France

Contacts

PRINCIPAL_INVESTIGATORFrançoise BRUCKER-DAVIS, PhD

Nice University Hospital

PRINCIPAL_INVESTIGATORSylvie HIERONIMUS, PhD

Nice University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026