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ior EPOCIM ® in the management of anemia of the preterm infant.Phase IV.

Phase 4
Completed
Conditions
Anemia of newborn preterm
Registration Number
RPCEC00000149
Lead Sponsor
Center of Molecular Immunology(CIM)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
121
Inclusion Criteria

1.Preterm patients with weight = 1500 g and gestational age < 34 weeks (determined by the method of date of last menstruation. 2.Patients whose parent or responsible family member has granted your consent to participation in the study in writing.
3.Patients with more than 15 days old.
4.Patients with an intake of at least 50 mL/kg/day of maternal and/or artificial milk.

Exclusion Criteria

1.Patients with diagnosis of hemorrhagic or hemolytic disease.
2.Patients with a diagnosis of major congenital malformation requiring transfer to another service of Neonatology.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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