Umbilical Cord Clamping and Infant Iron Status
Iron-deficiency Anemia
About this trial
This is an interventional prevention trial for Iron-deficiency Anemia focused on measuring Iron-deficiency anemia, Umbilical cord clamping, Infant
Eligibility Criteria
Inclusion Criteria: Pregnant women delivering at study site hospital Exclusion Criteria: Delivery by Cesarean section Pregnancy ≤ 36 or ≥ 42 weeks gestation Multiple gestation Diagnosis of any of the following in the current pregnancy: hemorrhage requiring clinic/hospital admission, placental abnormalities, fetal anomalies, Down's syndrome of the fetus Diagnosis of pre-eclampsia or eclampsia in current or previous pregnancies Diagnosis at any time for the mother of any of the following: Diabetes, hypertension, cardiopathies, chronic renal disease Infant with major congenital malformation Infant birth weight less than 2500 g Mother not planning to breast feed for at least 6 months Mother smoked during current pregnancy Unwilling to return for follow-up study visits at the hospital
Sites / Locations
- Hospital de Gineco Obstetrica #4 "Luis Castelazo Ayala" del Instituto Mexicano del Seguro Social
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Early umbilical cord clamping (control)
Delayed umbilical cord clamping
Umbilical cord was clamped immediately, or as close as possible, after delivery of the infant's shoulders. (This was standard practice in the study hospital, thus it served as the "control" group).
Umbilical cord was clamped at 2 minutes after delivery of the infant's shoulder's with the infant held at the level of the mother's uterus.