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Study identifier: NCT06990373 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Iron Status of Non-anemic Pregnant Women in First Trimester

Condition: Iron Deficiency (Without Anemia) · Reference Values · Iron Deficiency Without Anemia  ·  Sponsor: Hung Vuong Hospital

PhaseN/A
Planned participants600
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Huan Nguyen Pham, Master of medicine  ·  +849068844435  ·  huanpmd@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Hung Vuong HospitalHo Chi Minh City, Ho Chi Minh, VietnamRecruiting

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Source record: clinicaltrials.gov/study/NCT06990373