RecruitingNCT06990373

Iron Status of Non-anemic Pregnant Women in First Trimester

Establishment of Reference Intervals for Iron Test Panel for Pregnant Women at Hung Vuong Hospital


Sponsor

Hung Vuong Hospital

Enrollment

600 participants

Start Date

Mar 12, 2025

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with iron deficiency (without anemia) and reference values. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Hung Vuong Hospital

Ho Chi Minh City, Ho Chi Minh, Vietnam

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06990373


Related Trials