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Effects of oral Liposomal Iron Supplementation on anemic and non anemic Iron-Deficiency Children age 6 up to 59 months

Interventional Effects of oral Liposomal Iron Supplementation in anemic and non anemic Iron-Deficiency Preschool Children: A Randomized, Double-Blind, Placebo-Controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202401875833105
Enrollment
45
Registered
2024-01-09
Start date
2022-01-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Haematological Disorders Mental and Behavioural Disorders Nervous System Diseases Nutritional, Metabolic, Endocrine Paediatrics

Interventions

group c by liposomal iron
placebo

Sponsors

menoufia faculty of medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age range 6 months till 59 months old at baseline screenin c–reactive protein (CRP) is negative at the start and also in follow-up analysis, Hb concentration is 7.0 g/dl or above, and heart rate within normal range no history of consumption of iron supplements for 4 months ago or history of blood transfusion, if anemia is found, no other causes rather than ID are present, the child has no chronic or acute diseases (except for asthma) over the time of follow-up. no hemolytic anemia established diagnosed hemoglobinopathy (e.g., sickle cell disease, beta thalassemia major), or neurological disability as cerebral palsy, developmental delay or fits.

Exclusion criteria

Exclusion criteria: Children with a past history of prematurity, born small for date, or low birth weight below 2500 grams were excluded

Design outcomes

Primary

MeasureTime frame
to assess whether liposomal iron plus diet advice is superior to diet advice alone in terms of neurodevelopmental outcomes in children aged 6-59 months identified with NAID following screening.

Secondary

MeasureTime frame
to assess laboratory and anthropometric outcomes after intervention on anemic and NAID children.

Countries

Egypt

Contacts

Public Contactkerollos samaan

lecturer assisstant

kerosmn1@gmail.com201091481841

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026