Comparison of two inject able iron preparations for treatment of iron deficiency anemia in pregnancy
Not Applicable
- Conditions
- Health Condition 1: O251- Malnutrition in pregnancy
- Registration Number
- CTRI/2019/02/017553
- Lead Sponsor
- Department of Obstetrics and Gynecology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Antenatal women with (20-34 weeks ) gestation with diagnosed iron deficiency anemia of varying severity(Hb 6-9.9g/dl)
Singleton pregnancy
Exclusion Criteria
Hemodynamic instability or clinically perceived or anticipated need of blood transfusion
History of repeated blood transfusions
Haemoglobinopathies bleeding diathesis
Known history of asthma allergies hypersensitivity reactions eczema
History of hypersensitivity reaction to iron preparations
Advanced Systemic illnesses involving renal/hepatic /cardiovascular system
Conditions associated with iron overload viz thalessemia hemochromatosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement in anemia by hematological assessment at end of 4 weeks after IV Iron supplementation. <br/ ><br>Incidence of Local ADR /systemic ADRTimepoint: Improvement in anemia by hematological assessment at end of 4 weeks after IV Iron supplementation.
- Secondary Outcome Measures
Name Time Method Delivery-term/preterm <br/ ><br>NICU stay in days & reason <br/ ><br>Birth weight <br/ ><br>Cord blood hematology <br/ ><br>Timepoint: After Delivery