Iodine Deficiency Clinical Trial
— IOMUMOfficial title:
Iodine Status Monitoring in PortUguese Pregnant woMen: Impact of Supplementation
NCT number | NCT04010708 |
Other study ID # | IOMUM |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | April 17, 2018 |
Est. completion date | February 28, 2021 |
Verified date | July 2019 |
Source | Universidade do Porto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 485 |
Est. completion date | February 28, 2021 |
Est. primary completion date | September 30, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Pregnant women attending the 1st trimester fetal ultrasound scan, from the 10th to the 13th gestational week. Exclusion Criteria: - Use of Levothyroxine. |
Country | Name | City | State |
---|---|---|---|
Portugal | Faculty of Medicine of the University of Porto | Porto |
Lead Sponsor | Collaborator |
---|---|
Universidade do Porto | Centro de Investigação em Tecnologias e Serviços de Saúde (CINTESIS), Centro Hospitalar De São João, E.P.E., Faculty of Medicine (FMUP), Hospital de Braga, NOVA Medical School |
Portugal,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 1st trimester urinary iodine concentration | Median urinary iodine concentration at 1st trimester of gestation | Between gestational weeks 10 and 13 plus 6 days (one timepoint collection - Timepoint 1) | |
Primary | Rate of compliance to iodine supplementation guideline | Rate of compliance to iodine supplementation guideline at 1st trimester of gestation | Between gestational weeks 10 and 13 plus 6 days (one timepoint collection - Timepoint 1) | |
Secondary | Change in median iodine-to-creatinine ratio | Change in median iodine-to-creatinine ratio between 1st and 3rd trimesters of gestation | Up to 31 weeks | |
Secondary | Proportion of pregnant women with insufficient, adequate or excessive iodine intake | Classification of pregnant women by urinary iodine concentration levels according to WHO criteria (insufficient, adequate or excessive iodine intake) at 1st trimester of gestation. | Between gestational weeks 10 and 13 plus 6 days (one timepoint collection - Timepoint 1) | |
Secondary | Maternal median thyroglobulin | Maternal median thyroglobulin at 3rd trimester of gestation | Between gestational weeks 35 and 41 (one timepoint collection - Timepoint 2) | |
Secondary | 1st trimester mean sodium excretion | Mean sodium excretion at 1st trimester of gestation | Between gestational weeks 10 and 13 plus 6 days (one timepoint collection - Timepoint 1) | |
Secondary | 3rd trimester mean sodium excretion | Mean sodium excretion at 3rd trimester of gestation | Between gestational weeks 35 and 41 (one timepoint collection - Timepoint 2) |
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