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A study comparing parenteral with oral iron supplementation in pregnancy

Intravenous iron sucrose versus oral iron in treatment of iron deficiency anemia in pregnancy: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/11/004142
Enrollment
100
Registered
2013-11-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- pregnant women with Iron deficiency anemia

Interventions

Intervention1: Iron sucrose injections: In group B (intravenous group), women will be admitted for a short duration for the treatment. The total iron dose to be administered will be calculated as foll
0.24 is a correction factor taking into account the patientâ??s blood volume and hemoglobin iron content and 500 mg was for the restoration of iron stores. This total dose will be rounded up to the ne

Sponsors

Dr RPGMC Kangra HP
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age >18 years 2. Singleton pregnancy between 24â??34 weeks of gestation, 3. Moderate iron deficiency anemia (hemoglobin 7.0â??9.0 g/dL), 4. Mean corpuscular volume 5. Serum ferritin level 6. Negative naked eye single tube red cell osmotic fragility test (NESTROFT) 7. No associated obstetric or medical complications.

Exclusion criteria

Exclusion criteria: 1. Anemia due to any cause other than iron deficiency 2. Severe anemia (Hb 3. Asthma, viral hepatitis, cirrhosis, cardiovascular disease, autoimmune disease, suspected acute infection 4. Intolerance to iron derivatives 5. Women who had received parenteral iron treatment earlier (last 6 months) 6. Not willing to participate in the study

Design outcomes

Primary

MeasureTime frame
Primary outcome measure is efficacy of treatment, (determined by studying the rate of improvement in both the groups (by comparing the changes with the baseline values of Hb, MCV, MCH, MCHC and reticulocyte count on days 14, and 30. On day 30, changes in peripheral smear and serum ferritin will also be recorded.) Timepoint: from onset of treatment to delivery of baby

Secondary

MeasureTime frame
â?¢ Side effects profile â?¢ Neonatal outcome â?¢ Need for blood transfusion Timepoint: from onset of treatment to delivery of baby

Countries

India

Contacts

Public ContactChanderdeep Sharma

Dr RPGMC Kangra at Tanda (HP)

sureshsverma@gmail.com9418080404

Outcome results

None listed

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