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Iodine Supplementation During Pregnancy and Neuropsychological Development

NCT01049659 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 85

Last updated 2026-03-31

No results posted yet for this study

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.

Conditions

  • Healthy
  • Iodine Deficiency
  • Pregnancy

Interventions

BEHAVIORAL

Neuropsychological test

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

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Nice

    lead OTHER

Principal Investigators

  • Françoise BRUCKER-DAVIS, PhD · Nice University Hospital

  • Sylvie HIERONIMUS, PhD · Nice University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
23 Months
Max Age
25 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01049659 on ClinicalTrials.gov