Skip to main content
Clinical Trials/RPCEC00000149
RPCEC00000149
Completed
Phase 4

Evaluation of the safety and effectiveness of ior EPOCIM® in the management of anemia of the preterm infant.

Center of Molecular Immunology(CIM)0 sites121 target enrollmentFebruary 26, 2013

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Anemia of newborn preterm
Sponsor
Center of Molecular Immunology(CIM)
Enrollment
121
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 26, 2013
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Center of Molecular Immunology(CIM)

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

Similar Trials