Iodine Supplementation During Pregnancy and Neuropsychological Development
NCT01049659
Healthy, Iodine Deficiency
Nice, France
View Trial DetailsNCT Number: NCT03602404
The overall objective of this study is to develop a reliable method to obtain habitual iodine intakes from spot urinary iodine concentration (UIC) and to assess the prevalence of inadequate iodine intake in school-age children and women of reproductive age. We will evaluate different methods to estimate iodine intake from UIC and estimate the prevalence of inadequate and excess iodine intake in UIC studies conducted in populations with low, adequate and high iodine intakes using the the established estimated average requirement (EAR)/Tolerable Upper Intake Level (UL) cut-point method.
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Notify Me9 year–13 year
All sexes
Observational
University of Papua New Guinea, Sia, Morobe Province, Papua New Guinea
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Second arm: Women aged 18 - 49, exclusion / inclusion criteria apply, plus non-pregnant, non-lactating.
Time frame: 17 months
Estimated daily iodine intake of the study population derived from urinary iodine and creatinine concentrations measured in spot urine samples
Time frame: 17 months
Measured in spot urine samples and 24 h urine collections
Time frame: 17 months
Measured in spot urine samples and 24 h urine collections
Swiss Federal Institute of Technology
Other
Estimating the Usual Iodine Intake From Spot Urinary Iodine Concentrations to Obtain the Prevalence of Inadequate or Excess Iodine Intake in School-aged Children and Adults
Acronym: ITURN
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