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Comparison of serum ferritin level guided and standard practice of oral iron supplementation in very preterm neonates

Not Applicable
Conditions
Health Condition 1: P073- Preterm [premature] newborn [other]
Registration Number
CTRI/2024/05/066651
Lead Sponsor
Rainbow Children s Hospital and Birthright .
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Neonates less than 32 weeks of gestational age hospitalized in NIC

Exclusion Criteria

Preterm neonates whom iron supplementation is deferred because as in

1.Those with an active, culture-proven infection, or positive sepsis screen

2.A major surgical malformation of gut

3.Neonates in whom bowel resection is done

4.Neonates with Stage II and III Necrotizing enterocolitis

5.Cyanotic congenital heart disease

6.Neonates with hemoglobinopathies.

7.Neonates diagnosed with inflammatory conditions like hemophagocytic lymphohistiosis (HLH).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Determining the optimal age (in day of life) for initiation of oral iron supplementation at the time of full feed achievement and at 2 weeks of life (whichever is later) by serum ferritin monitoring compared with the standard practice.Timepoint: 2 weeks to 4 weeks
Secondary Outcome Measures
NameTimeMethod
1.Total quantum (in mg) of oral iron supplemented during the NICU stay. <br/ ><br>2.Number of LRBC transfusions administered during their stay in NICU. <br/ ><br>3.Mean serum ferritin levels at the time of discharge in both groups. <br/ ><br>Timepoint: At discharge (8-10 weeks)
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