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Comparison of intravenous iron with blood transfusion for anemia in postpartum women.

Comparison of intravenous iron isomaltoside versus blood transfusion for treatment of moderate anemia in postpartum women:A Randomised controlled trial. - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055752
Enrollment
56
Registered
2023-07-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Comparison of intravenous iron isomaltoside versus blood transfusion for the treatment of moderate anemia in postpartum women.: The Iv iron group will receive Intravenous iron isomaltos

Sponsors

Rajendra institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. women clinically anemic or complicated with anemic symptoms irrespective of mode of delivery with hemoglobin measured 12hrs after delivery ranging between 7-9g/dl. 2. women who are willing to participate in the study and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Women with hemodynamic instability. 2. Women with history of Blood transfusion during pregnancy or after delivery 3. Women with multiple allergies,or any acute infection. 4. Women with any hemoglobinopathies.or hemolytic anemia or any chronic illness like chronic liver disease, chronic kidney disese, HELLP syndrome etc. 5. Women with history of adverse events following any injectable iron preparations in the past. 6. Women with known case of iron overload or disturbance in iron absorption eg.Hemochromatosis, Hemosiderosis.

Design outcomes

Primary

MeasureTime frame
To compare the effectiveness of intravenous iron isomaltoside vs blood transfusion in treatment of moderate anemia in postpartum females.Timepoint: At baseline,3rd week and 6th week.

Secondary

MeasureTime frame
To compare the number ,type of adverse effects with iv iron isomaltoside vs blood transfusion.Timepoint: Day 1 ,6th week

Countries

India

Contacts

Public ContactKritika Srivastava

Rims,Ranchi

drkritika25@gmail.com7209907001

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026