Iron Status of Non-anemic Pregnant Women in First Trimester
Recruiting
Observational Study
Iron Deficiency (Without Anemia)
Reference Values
Iron Deficiency Without Anemia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Observational
- Participants needed
- 600 (estimated)
- Sponsor
- Hung Vuong Hospital · Other
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About This Trial
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 exclu…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women attending antenatal care, carrying a single live fetus.
* Systolic blood pressure at the time of examination \< 140 mmHg.
* Diastolic blood pressure at the time of examination \< 90 mmHg.
* Body temperature at the time of examination between \>35°C and \<37.5°C.…
Contacts