Using NIRS to Evaluate Splanchnic Oxygenation During Blood Transfusion in Preterm Infant
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorGadjah Mada University
About this trial
To evaluate the differences splanchnic oxygen saturation in preterm infants receiving red blood cell transfusion with and without enteral feeding, and their outcomes.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Infant with gestational age < 37 weeks
Planned to receive blood transfusion
Had received minimum 25 ml/kg/day enteral feeding
in stable condition
Disqualifiers
Infant with multiple congenital anomalies
Infant with suspected/confirmed genetic anomalies
Parents or family did not sign the informed consent
Trial design
Design model
Single group
Treatments tested in this trial
Enteral feeding
Dietary supplementintervention group received enteral feeding breastmilk during transfusion
Treatment groups
42 Participants
are divided into 2 treatment groupsGroup A: control group not received enteral feedingNo intervention 0 interventions
Group B: intervention group received enteral feedingActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
cerebral splanchnic oxygenation ratio using nirs
percentage of splanchnic oxygenaation divided with cerebral oxygenation
Time frame
from enrollment to 48 hours after transfusionSponsors 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: