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Measurement of Cerebral and Peripheric Tissue Oxygenation in Anemic Preterm Infants Who Underwent Blood Transfusion

Measurement of Cerebral and Peripheric Tissue Oxygenation in Anemic Preterm Infants Who Underwent Blood Transfusion:A Near Infrared Spectroscopy Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01251068
Enrollment
40
Registered
2010-12-01
Start date
2010-12-31
Completion date
2011-06-30
Last updated
2010-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemic Preterms, Cerebral Oxygenation,Somatic Oxygenation,Blood Transfusion

Keywords

anemic preterms, cerebral oxygenation,somatic oxygenation, blood transfusion

Brief summary

Near infrared spectroscopy offers the possibility of noninvasive and continuous bedside investigation of cerebral oxygenation in newborn infants. Using this technique we investigated the relationship between changes in cerebral oxygenation and hemodynamics, and changes in some physiological variables during blood transfusion in anaemic preterm infants.

Interventions

NIRS device used in this study, the optical field includes a volume of tissue approximately 2 cm deep to the surface probe with a 4-mm source-detector distance, and thus, organ-specific monitoring is feasible in small patients. With informed consent, we applied NIRS probes to the forehead and the lower extremity for cerebral (rSO2C) and peripheric (rSO2P) regional oxygen saturation measurements.

DEVICEnear infrared spectroscopy device

NIRS device used in this study, the optical field includes a volume of tissue approximately 2 cm deep to the surface probe with a 4-mm source-detector distance, and thus, organ-specific monitoring is feasible in small patients. With informed consent, we applied NIRS probes to the forehead and the lower extremity for cerebral (rSO2C) and peripheric (rSO2P) regional oxygen saturation measurements.

Sponsors

Zekai Tahir Burak Women's Health Research and Education Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Days to No maximum
Healthy volunteers
No

Inclusion criteria

\<32 gestational age and/or \<1500gr.,\>30th day preterm infants -

Exclusion criteria

sepsis,shock,severe intracranial hemorrhage,NEC,abdominal and cranial surgery \-

Design outcomes

Primary

MeasureTime frame
Cerebral and peripheric oxygenation measurements in anemic preterm infants.6 months

Countries

Turkey (Türkiye)

Contacts

Primary Contactgonca sandal, MD
kocabasgonca@mynet.com05054871028

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026