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Iron Status of Non-anemic Pregnant Women in First Trimester

NCT06990373 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2025-05-30

No results posted yet for this study

Summary

This cross-sectional study aims to establish reference intervals for iron biomarkers-including serum iron, ferritin, total iron-binding capacity (TIBC), and transferrin saturation (TSAT)-in healthy pregnant women during the first trimester. Additionally, the study will investigate the current prevalence of non-anemic iron deficiency (NAID) in this population. By applying strict inclusion and exclusion criteria to eliminate potential confounding factors, the study seeks to provide a reliable baseline for evaluating iron status and early detection of iron deficiency without anemia among pregnant women.

Conditions

  • Iron Deficiency (Without Anemia)
  • Reference Values
  • Iron Deficiency Without Anemia

Sponsors & Collaborators

  • Hung Vuong Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-12
Primary Completion
2025-06-30
Completion
2025-08-30

Countries

  • Vietnam

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06990373 on ClinicalTrials.gov