The effect of supplemental iron elimination on pregnancy outcome
Not Applicable
- Conditions
- pregnancy outcome.Pregnancy-related condition, unspecified
- Registration Number
- IRCT201101115563N1
- Lead Sponsor
- Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 960
Inclusion Criteria
women who were at the first trimester of pregnancy with single fetus, Hb > 12 gr/dl, not receiving iron containing supplements in the last month, BP < 140/90 mmHg,
Exclusion criteria: Hb less than 10.5 gr/dl or less than 11 gr/dl at the end of 2nd and 3rd trimesters respectively, miscarriage of current pregnancy, abnormality of the fetus, loss to follow-up
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preeclampsia. Timepoint: before intervention and every month during pregnancy. Method of measurement: blood pressure checking and urine protein test.;Preterm labor. Timepoint: every month after 20 w of pregnancy. Method of measurement: control of uterine contractions and cervical examination.;PROM. Timepoint: monthly prenatal care. Method of measurement: declaring membrane rupture by patient and nitrazin test.;Neonatal birth weight. Timepoint: immediately after birth. Method of measurement: by precise scale.
- Secondary Outcome Measures
Name Time Method Maternal anemia. Timepoint: monthly prenatal care. Method of measurement: Hb,Hct test.