Clinical Trials in Egypt / NCT06871917
Starting soon
Observational
Maternal Iron Deficiency and/or Iron Deficiency Anemia to Neonatal Hemoglobin Concentration and Iron Stores
NCT06871917 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Relation, Mother-Child
Study summary
study the relationship between maternal iron deficiency (ID) and/or iron deficiency anemia (IDA) to neonatal hemoglobin concentration and iron stores at birth
Eligibility
Inclusion Criteria:
* All pregnant women and their infant pairs who have given consent to participate.
* Mothers Age: 21-40 years' old.
* Term infants (37-42 weeks of gestation) with birth weight ≥2500 g born to mothers who had an uncomplicated normal singleton vaginal delivery or caesarian section delivery was included.
Exclusion Criteria:
* Mothers with a history of antepartum hemorrhage, pre-mature labor pain, high-risk pregnancy (eg. history of trauma and severe infection during pregnancy), severe hyperemesis, pre-eclampsia severe anemia requiring blood transfusion, and any chronic medical illnesses as: gestational diabetes, hypertension, hypothyroidism, epilepsy, liver disease, renal disease cardiorespiratory disease, immunodeficiency syndrome, and hematological (other causes of anemia)
* infants who suspected with congenital and/or chromosomal anomalies and pathological jaundice, also multiple pregnancy was excluded from the study.
* Mothers withdrew from given a written consent will be excluded from the study.
Primary outcome measure(s)
- Evaluation the effect of maternal iron deficiency (ID) and/or iron deficiency anemia (IDA) to fetal haemoglobin concentration and fetal iron stores. — 2 years
evaluation the correlation between ID and IDA in maternal and neonatal samples
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Naglaa Ali Ali | Asyut | Egypt |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06871917 on ClinicalTrials.gov ↗ ← All trials in Egypt