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Comparison of conventional iron vs liposomal iron preparation for treating iron deficiency anemia in pregnancy.

Effectiveness and tolerability of liposomal iron compared to conventional iron supplementation in treating iron deficiency anemia in antenatal women a randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096237
Enrollment
120
Registered
2025-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O990- Anemia complicating pregnancy, childbirth and the puerperium Health Condition 2: D509- Iron deficiency anemia, unspecified

Interventions

Intervention1: Liposomal iron – 29 mg elemental iron per tablet: Liposomal iron is a form of oral iron supplement where the iron is encapsulated within liposomes. This liposomal delivery system protec

Sponsors

Department of Pharmacology Institute of Post Graduate Medical Education And Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pregnant women aged at least 18 years. Gestational age at least 14 weeks (second trimester). Diagnosed with iron deficiency anemia (Hb 7.0 to 10.5 g/dL with other parameters suggestive of iron deficiency) Willing to provide written informed consent and adhere to study.

Exclusion criteria

Exclusion criteria: Severe anemia (Hb less than 7 g/dL) Requirement of parenteral iron. History of hookworm infestation or chronic bleeding from any source. Known hemoglobinopathies (For example thalassemia, sickle cell anemia). Gastrointestinal disorders affecting iron absorption. History of allergy to oral iron supplements. Co-existing chronic illnesses (For example chronic kidney disease, malignancy, chronic liver disease) likely to affect response to oral iron therapy). Received parenteral iron therapy within last 3 months.

Design outcomes

Primary

MeasureTime frame
Increase in hemoglobin by 2 gm/ dl after treatmentTimepoint: Participants will be followed up at 4, 8, and 12 weeks post enrolment

Secondary

MeasureTime frame
Changes in serum iron, total iron binding capacity, transferrin saturation. Changes in PCV, RBC indices (MCV, MCH, MCHC) and peripheral red cell morphology.Timepoint: Participants will be followed up at 12 weeks post enrolment

Countries

India

Contacts

Public ContactDR AVIJIT HAZRA

IPGMER and SSKM Hospital

blowfans@yahoo.co.in9831188172

Outcome results

None listed

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