Effect of prophylactic iron supplementation on Pregnancy outcome
Not Applicable
- Conditions
- Iron supplementation in pregnant women.
- Registration Number
- IRCT138706141196N1
- Lead Sponsor
- lorestan university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 166
Inclusion Criteria
inclusion criteria: GA: <20 weeks, Age:18-24 y,gravidity 1, BMI:18.5-24.9 kg/m2, Hb>110g/l, Serum Ferritin >20Ug/l
Exclusion criteria: Hb<110g/l, infection, disease,
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Serum ferritin. Timepoint: biggining the study(<20 wk), 28 wk of gestation and 38 wk of gestation. Method of measurement: radioimiunoassay method.;Hemoglobin. Timepoint: biggining the study(<20 wk), 28 wk of gestation and 38 wk of gestation. Method of measurement: cyanid hemoglobin.;Fasting blood sugar. Timepoint: biggining the study(<20 wk), 28 wk of gestation and 38 wk of gestation. Method of measurement: Glocose oxidaze.;Birth weight. Timepoint: at birthday. Method of measurement: recording weight by scale.;Birth length. Timepoint: at birthday. Method of measurement: strip meter.;Gestational age. Timepoint: at birthday. Method of measurement: calculated from the number of completed weeks since the first day of the mother's last menstrual period to the date of birth.
- Secondary Outcome Measures
Name Time Method Maternal weight gain. Timepoint: at delivery. Method of measurement: The difference between mothers' weight before pregnancy and after delivery.;Adherence to iron supplementation. Timepoint: at each return visiting by physician. Method of measurement: calculated on the basis of the number of tablets remaining in the box.