Thyroid Function Throughout Pregnancy With and Without Iodine Supplementation

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Completed
CT.gov ID
NCT00831402
Collaborator
(none)
111
1
2
14
7.9

Study Details

Study Description

Brief Summary

Goals of the study :
  1. To study maternal thyroid function during pregnancy with or without supplementation with pregnancy tablets fortified with iodine

  2. To establish reference values of thyroid function at different stages of pregnancy (3 trimesters)

  3. To precise screening strategy of iodine deficiency in our population and suggest recommendation for its prevention.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Oligobs Maxiode
  • Dietary Supplement: controll group
N/A

Detailed Description

Overt maternal hypothyroidism and/or iodine deficiency during pregnancy are linked to mental retardation in their offspring. Iodine deficiency may lead to maternal hypothyroxinemia, and even mild hypothyroidism in predisposed women. Indeed, thyroid hormones are of paramount importance for fetal brain development. During the first trimester of pregnancy, the only thyroid hormones available to the fetus are from maternal origin. Later in pregnancy, fetal thyroid progressively starts producing thyroid hormone, providing that maternal iodine status is adequate (≥200-250 mcg/day). It has been shown recently that mild maternal hypothyroidism may be responsible for discrete neuropsychological impairment in her child, implying a potential benefit for early screening and care during pregnancy. Furthermore, iodine deficiency is extremely common in our area (Brucker-Davis et al 2004). However, there is no official recommendation for screening and prevention, as for gestational diabetes for example.

We propose to study healthy pregnant women, screened before 12 weeks of gestation and without thyroid disease. They will be randomized in 2 groups and will therefore take pregnancy tablets, iodine fortified or not (Oligobs Maxiode -150 mcg/j of iodine, vs Oligobs grossesse), in addition to appropriate nutritional advice. Their longitudinal study will involve:

  1. Evolution of thyroid function parameters in the 2 groups, with comparison of maternal thyroid volumes, maternal thyroid hormones levels and cord blood parameters, including thyroglobulin, during pregnancy and in postpartum.

  2. Establishment of reference ranges for thyroid parameters for each trimester of pregnancy.

This public health project rests on our expertise in the care of pregnancies with maternal endocrine and metabolic disease (Hieronimus et al 2003-2005) and on a close collaboration of our Departments within the Pole "Mother-Child", conveniently located at the same hospital. It will allow us to precise iodine deficiency screening and prevention in our population and to structure and optimize the care for women with thyroid disease screened early in pregnancy (opening of a specific clinic), in order to improve maternal and fetal prognosis

Study Design

Study Type:
Interventional
Actual Enrollment :
111 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Assessment of Thyroid Function Throughout Pregnancy With and Without Iodine Supplementation
Study Start Date :
Jun 1, 2007
Actual Primary Completion Date :
Jul 1, 2007
Actual Study Completion Date :
Aug 1, 2008

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Arm without iodized vitamin (VITAMIN OLIGOBS PREGNANCY)

50 women will be studied in the absence of iodized supplémentation(natural history of function thyroïdienne in the course of the pregnancy and in the post partum)

Dietary Supplement: controll group
50 women will be studied in the absence of iodized supplémentation(natural history of function thyroïdienne in the course of the pregnancy and in the post partum)

Active Comparator: Arm with iodized vitamin

The 50 women will be follow up with a supplémentation iodized by vitamins of pregnancy strengthened in iodin everything in the course of the pregnancy and during the 3 months post partum (Oligobs Maxiode, 150 mcg / of iodizes, is 2cp a day)

Dietary Supplement: Oligobs Maxiode
The 50 women will be follow up with a supplémentation iodized by vitamins of pregnancy strengthened in iodin everything in the course of the pregnancy and during the 3 months post partum (Oligobs Maxiode, 150 mcg / of iodizes, is 2cp a day)

Outcome Measures

Primary Outcome Measures

  1. • Intra individual variation of maternal thyroglobulin between the first trimester and the delivery • And cord blood thyroglobulin With comparison of the 2 groups (control and supplementation with iodine) [Every 3 months up to the give birth, the day of a give birth, and after three months]

Secondary Outcome Measures

  1. Comparison of control and treated groups for : • Frequence of miscarriage, duration of gestation, birth weight, APGAR, neonatal complications, Maternal thyroid function, Frequency of post partum thyroiditis,Cord blood thyroid function [Every 3 months up to the give birth, the day of a give birth, and after three months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All women follow-up in the three months of the pregnancy in the CHU de Nice

  • Maternal thyroid function is between and 0.1<TSH<2.5 mUI/l, 23>T4L>12 pmol/l

  • Person over 18

  • Signed lit Consent

  • Give birth in the CHU of Nice

Exclusion Criteria:
  • Allergy known in iodine

  • Iodized surcharge defined by an iodurie> 400 mcg / l

  • Catch of ongoing iodized vitamins of pregnancy

  • Participation in another research protocol

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Nice - 4 avenue Reine Victoria - Hôpital de Cimiez Nice Alpes-Maritimes France 06001

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Françoise Dr BRUCKER-DAVIS, PH, CHU de Nice - Service d'endocrinologie - Hôpital de l'Archet - 151 Route de saint-antoine de ginestière 06200 Nice

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT00831402
Other Study ID Numbers:
  • 05-PHRC-03
First Posted:
Jan 29, 2009
Last Update Posted:
Mar 26, 2012
Last Verified:
Feb 1, 2009
Keywords provided by Centre Hospitalier Universitaire de Nice

Study Results

No Results Posted as of Mar 26, 2012