Risk Factors and Clinical Outcomes of Neonatal Anemia in NICU
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-30
SponsorAssiut University
About this trial
Risk Factors, and Clinical Outcomes of Neonatal Anemia in the NICU of a Tertiary Care Hospital
Eligibility criteria
This trial accepts healthy volunteersQualifiers
All live-born neonates admitted to the NICU within the first 24 hours of life.
Both term and preterm infants.
Disqualifiers
Major congenital malformations
Chromosomal abnormalities or genetic syndromes
Neonates with a previous blood transfusion before study enrollment
Trial population
neonates
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Understanding the local prevalence, associated factors, and outcomes of neonatal anemia
To determine the prevalence of neonatal anemia among neonates admitted to a tertiary care neonatal intensive care unit (NICU * To identify maternal, perinatal, and neonatal risk factors associated with neonatal anemia * To assess short-term outcomes, including length of hospital stay, need for blood transfusion, morbidity, and mortality
Time frame
1 yearLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: