CClinicalTrials.gg
CompletedNCT02312466SISUpdated Sep 16, 2020

Swiss National Iodine Survey 2015

An observational study in Healthy Subjects, sponsored by Isabelle Herter-Aeberli. Completed at 1 site in Switzerland. Open to participants aged 6 Years to 44 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-09-16.

Sponsored by Isabelle Herter-Aeberli · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,430
Ages
6 Years to 44 Years
Sex
All
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Study summary

The aim of this study is to monitor iodine nutrition in Switzerland in order to inform the authorities regarding iodine content in iodized salt. As a proxy for the entire population the investigators will study school aged children, pregnant women and women of reproduction age.

Read the detailed description

In a national sample of school aged children (n=990), pregnant women (n=700) and women of reproductive age (n=700) urinary iodine will be determined in order to assess iodine nutrition in Switzerland. In addition, in both groups of women a blood sample will be taken for the determination of thyroid hormones, iron- and folate status. Questionnaires will be used for the determination of dietary iodine and salt intake as well as sociodemographic parameters.

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Conditions studied

  • Healthy Subjects
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In context

Lead sponsor

Isabelle Herter-Aeberli is the lead sponsor of 13 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
6 Years to 44 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

school aged children, 6-12 years pregnant women, 18-44 years women of reproductive age, 18-44 years

Inclusion criteria

  • Healthy
  • Living in Switzerland for at least 1 year
  • For pregnant women: singleton pregnancy

Exclusion criteria

Exclusion Criteria:

  • Major known medical illness: thyroid dysfunction, gastrointestinal or metabolic disorders and taking chronic medications
  • For women of reproductive age: pregnancy, breastfeeding
  • Use of X-ray or CT contrast agent or iodine containing medication within the past year
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,430 participants (actual)
Patient registry
No

Groups and cohorts

  • School aged children
  • Pregnant women
  • Women of reproductive age
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What researchers measure

Primary outcomes

  1. Median urinary iodine concentration in school aged children, pregnant women and women of reproductive age

    analysis of urine samples

    Time frame: Baseline

Secondary outcomes

  1. Population mean thyroglobulin

    Analysis of venous blood samples. Assessed only in women

    Time frame: Baseline

  2. Population mean thyroid stimulating hormone

    Analysis of venous blood samples. Assessed only in women

    Time frame: Baseline

  3. Population mean thyroxine

    Analysis of venous blood samples. Assessed only in women

    Time frame: Baseline

  4. Median urinary sodium concentration

    Time frame: Baseline

  5. Median urinary creatinin concentration

    Time frame: Baseline

Other outcomes

  1. Mean height of school aged children and women of reproductive age

    Time frame: Baseline

  2. Mean weight of school aged children and women of reproductive age

    Time frame: Baseline

  3. Median urinary fluoride

    Analyzed in urine samples from school aged children only.

    Time frame: Baseline

  4. Population mean folate status

    Analysis of red blood cell folate and plasma folate in venous blood samples.

    Time frame: Baseline

  5. Populations mean iron status

    Serum analysis: ferritin, transferrin receptor; in women of reproductive age and pregnant women.

    Time frame: Baseline

  6. Individual inflammatory state

    Serum analysis of CRP and AGP, analyzed only in women

    Time frame: Baseline

  7. Intake of iodine in micro grams per day

    iodine intake assessed by food frequency questionnaire, only in women

    Time frame: Baseline

  8. % of households with adequate iodine coverage

    Salt samples only collected from children (subgroup)

    Time frame: Baseline

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Study locations

1 site
  • Human Nutrition Laboratory, ETH Zurich
    Zurich, 8092, Switzerland
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References and documents

Publications

  • Andersson M, Hunziker S, Fingerhut R, Zimmermann MB, Herter-Aeberli I. Effectiveness of increased salt iodine concentration on iodine status: trend analysis of cross-sectional national studies in Switzerland. Eur J Nutr. 2020 Mar;59(2):581-593. doi: 10.1007/s00394-019-01927-4. Epub 2019 Mar 1. PubMed 30843107 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02312466
Lead sponsor
Isabelle Herter-Aeberli
Collaborators
Federal Food Safety and Veterinary Office (Switzerland)
Responsible party
Isabelle Herter-Aeberli (PhD, Swiss Federal Institute of Technology) — Sponsor-investigator
First posted
Dec 9, 2014
Start date
Mar 2015
Primary completion
Sep 2016
Completion
Dec 2016
Last update
Sep 16, 2020
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2020. You cannot join it, but the record below documents what was studied.

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