Iodine Status Monitoring in PortUguese Pregnant woMen: Impact of Supplementation

NCT04010708 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 485

Last updated 2023-10-19

No results posted yet for this study

Summary

Data from 2007 regarding iodine status among Portuguese pregnant women indicate this is an iodine deficient population group, with only 16.8% presenting adequate urinary iodine values. This may have serious implications for normal cognitive development of the offspring and a concerning socioeconomic impact. In 2013, concerns by the Portuguese Directorate-General of Health lead to the implementation of a public health policy (nº 011/2013) recommending iodine supplementation during pregnancy. IoMum emerges from this context to monitor and update iodine status in Portuguese pregnant women and to evaluate the effectiveness of the above policy by assessing clinical compliance to iodine supplementation and the impact of iodine supplementation in this vulnerable group. IoMum will update data on iodine nutrition in Portuguese pregnant women, promoting political actions towards the elimination of iodine deficiency and thus to the reduction of nutritional, social and economic inequalities.

Conditions

  • Iodine Status in Pregnancy
  • Iodine Deficiency

Interventions

DIAGNOSTIC_TEST

Urinary Iodine Concentration Measurement

UIC

Sponsors & Collaborators

  • NOVA Medical School

    collaborator OTHER
  • Centro Hospitalar De São João, E.P.E.

    collaborator OTHER
  • Hospital de Braga

    collaborator OTHER
  • Centro de Investigação em Tecnologias e Serviços de Saúde

    collaborator OTHER
  • Universidade do Porto

    lead OTHER

Principal Investigators

  • Elisa Keating, PhD · Center for Health Technology and Services Research

  • Conceição Calhau, PhD · Center for Health Technology and Services Research

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-17
Primary Completion
2020-09-30
Completion
2021-02-28

Countries

  • Portugal

Study Locations

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Read the full study record

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View NCT04010708 on ClinicalTrials.gov