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Using NIRS to Evaluate Splanchnic Oxygenation During Blood Transfusion in Preterm Infant

G

Gadjah Mada University

Status

Not yet enrolling

Conditions

PreTerm Neonate
Enteral Feeds
Splanchnic Oxygenation
NIRS

Treatments

Dietary Supplement: Enteral feeding

Study type

Interventional

Funder types

Other

Identifiers

NCT06663085
KE/FK/1583/EC/2024

Details and patient eligibility

About

To evaluate the differences splanchnic oxygen saturation in preterm infants receiving red blood cell transfusion with and without enteral feeding, and their outcomes.

Full description

using NIRS to evaluate splanchnic oxygenation

Enrollment

42 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Infant with gestational age < 37 weeks
  • Planned to receive blood transfusion
  • Had received minimum 25 ml/kg/day enteral feeding
  • in stable condition

Exclusion criteria

  • Infant with multiple congenital anomalies
  • Infant with suspected/confirmed genetic anomalies
  • Parents or family did not sign the informed consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

42 participants in 2 patient groups

control group not received enteral feeding
No Intervention group
Description:
control group not received enteral feeding during blood transfusion
intervention group received enteral feeding
Active Comparator group
Description:
intervention group still received enteral feeding during blood transfusion
Treatment:
Dietary Supplement: Enteral feeding

Trial contacts and locations

1

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Central trial contact

leksmana hidayatullah, medical doctor

Data sourced from clinicaltrials.gov

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