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A Study comparing Biomarker guided Oral Iron supplementation versus routine oral iron supplementation in managing patients with Iron Deficiency Anaemia

Hepcidin-Guided Oral Iron Therapy Versus Standard of Care in the Management of Iron Deficiency Anaemia A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107396
Enrollment
90
Registered
2026-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: D508- Other iron deficiency anemias

Interventions

Intervention1: Hepcidin guided oral iron therapy: In one group Serum hepcidin will be tested and low hepcidin group will receive daily iron and high hepcidin group will receive alternate day iron. In

Sponsors

All India Institute of Medical Sciences, Madurai, Tamil Nadu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults between 18 to 60 years with confirmed IDA (Hb less than 13 g per dL in males, less than 12 g per dL in females ferritin less than 30 ng per mL or ferritin between 30 and 100 ng per mL with TSAT less than 20) will be included.

Exclusion criteria

Exclusion criteria: Chronic kidney disease stage less than 3 (eGFR less than 60 mL per min per 1.73 m ) Decompensated chronic liver disease Known hemoglobinopathies Pregnancy or lactation Recent blood transfusion (within 4 weeks) Active infection/inflammation Use of parenteral iron in last 3 months Ongoing oral iron supplements

Design outcomes

Primary

MeasureTime frame
Change in hemoglobin (Hb, g/dL) from baseline to 8 weeks. Iron indices, hepcidin correlation and change, adherence, GI side effects, responder proportion, and cost-effectiveness. Timepoint: At baseline, 4 weeks and 8 weeks

Secondary

MeasureTime frame
Iron indices, hepcidin correlation & change, adherence, GI side effects, responder proportion, & cost effectiveness. Timepoint: At baseline, 4 weeks & 8 weeks

Countries

India

Contacts

Public ContactDr Konnepati Sushma

All India Institute of Medical Sciences, Madurai, Tamil Nadu

sushmakonnepati@gmail.com9490354025

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026