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Completed

NCT Number: NCT00791466

Maternal Iodine Supplementation and Effects on Thyroid Function and Child Development

Rationale: In regions of severe endemic goiter, the adverse effects of in utero iodine deficiency on neuromotor development are well established: randomized controlled trials of iodine supplements given to iodine deficient mothers before pregnancy or during early pregnancy improve motor and cognitive performance of their offspring. However, the potential adverse effects of mild-to-moderate iodine deficiency during pregnancy are unclear. Inadequate thyroid function in the fetus and newborn are the likely cause of brain damage in iodine deficiency.

Objective: To determine whether the daily oral administration of 200 µg iodine to pregnant women in areas of mild-to-moderate iodine deficiency improves maternal and newborn thyroid function, pregnancy outcome, birth weight, infant growth and cognitive performance.

Study design: Double-blind randomized controlled multicentre trial. Study population: Pregnant women (18-40 years) presenting at the clinic for their first prenatal visit will be recruited at two research sites, namely St. Martha's hospital in Bangalore, India and Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. At each site, 400 women will be recruited.

Intervention: Half of the women will be randomized to iodine treatment (200 µg per day) and the other half to placebo throughout pregnancy.

Main study parameters/endpoints: Differences between group means in indicators of thyroid function, birth outcome, urinary iodine, breast milk iodine, infant growth, and psychomotor development.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

St. Johns Medical College and Research Institute, Bangalore, India

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-40 years;
  • Gestational age: ≤ 14 weeks (as judged by the date of the last menstrual period);
  • Single pregnancy;
  • Non-lactating;
  • Planned residence in the area for the duration of the study (3 years).

Exclusion criteria

  • TSH levels outside the normal range
  • History of serious medical conditions such as HIV, hypertension, diabetes, renal, hepatic or cardiovascular disease, thyroid disorders, mental disorders;
  • Use of iodine supplement.

Treatment and study plan

Placebo

Dietary Supplement

Daily placebo supplementation from enrolment <14 wk of gestation until delivery

Iodine

Dietary Supplement

Daily supplementation with 200 µg iodine from enrolment <14 wk of gestation until delivery

Primary outcomes

  1. Current primary outcome: Infant cognitive and motor development

    Time frame: Regular intervals up till 6 years of age

  2. Original primary outcome: Maternal thyroid function

    Time frame: 3-month intervals during pregnancy, at delivery

Secondary outcomes

  1. Birth outcome

    Time frame: At delivery

  2. Maternal and infant urinary iodine

    Time frame: Regular intervals during pregnancy up till 2 years after delivery

  3. Breast milk iodine

    Time frame: 3 and 6 months after delivery

  4. Long-term follow up

    Time frame: Child age 2-6 years

    Anthropometrics, urinary iodine, thyroid hormones, WPPS, BRIEF-P, hearing thresholds

Sponsors and collaborators

Lead sponsor

Wageningen University

Other

Collaborators

  • Mahidol University
  • Nestlé Foundation
  • St. John's Research Institute
  • Swiss National Science Foundation
  • Unilever R&D

Registry information

Official study title

Iodine Supplementation in Pregnant Women Living in Mild-to-moderately Iodine Deficient Areas in India and Thailand: Effects on Pregnancy Outcome and Infant Development

Acronym: MITCH

Important dates

Study start
2008
Primary completion
2012
Study completion
2016
First posted
Nov 14, 2008
Registry last updated
Nov 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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