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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03274726
Other study ID # CDC-NCCDPHP-2011-17
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 1999
Est. completion date December 1, 2010

Study information

Verified date May 2024
Source Centers for Disease Control and Prevention
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This analysis describes the distribution of TBI and the prevalence of iron deficiency (ID) and iron deficiency anemia (IDA) among toddlers, non-pregnant women, and pregnant women.


Description:

Background: Total body iron stores (TBI), which are calculated from serum ferritin (SF) and soluble transferrin receptor (sTfR) concentrations, can be used to assess the iron status of populations in the United States. Objective: This analysis describes the distribution of TBI and the prevalence of iron deficiency (ID) and iron deficiency anemia (IDA) among toddlers, non-pregnant women, and pregnant women. Design: Investigators analyzed data from NHANES; toddlers aged 12-23 mo (NHANES 2003-2010), non-pregnant women aged 15-49 y (NHANES 2007-2010), and pregnant women aged 12-49 y (NHANES 1999-2010). Investigators used SAS survey procedures to plot distributions of TBI and produce prevalence estimates of ID and IDA for each target population. All analyses were weighted to account for the complex survey design


Recruitment information / eligibility

Status Completed
Enrollment 5000
Est. completion date December 1, 2010
Est. primary completion date December 1, 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Months to 49 Years
Eligibility Included: - Children ages 12-23 months and Women ages 12-49 years - Those who completed the MEC Excluded: - Those missing data on iron biomarkers

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centers for Disease Control and Prevention

Outcome

Type Measure Description Time frame Safety issue
Primary Iron Deficiency Total Body Iron <0 mg/kg 1999-2010
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