Clinical Trials Logo

Clinical Trial Summary

Premature babies have to deal with many problems from the moment they are born due to the immature of their organs. Their clinical condition is unstable, especially in the first few weeks, and they are greatly affected by environmental factors. During this period, blood transfusion may be needed for many reasons such as intraventricular hemorrhage and necrotizing enterocolitis. In addition, multiple blood draws to evaluate irregular metabolic, hematological and biochemical findings result in anemia and the need for blood transfusion. There are many algorithms regarding blood transfusion indications and transfusion limits in premature babies. However, there are no strict rules regarding the application of warming before blood transfusion, but it is recommended by some guidelines. Especially in unstable babies such as advanced premature babies, it is recommended to give blood by heating it at physiological temperature to avoid important complications such as hypothermia, coagulopathy and rhythm disturbances. Premature babies, whose hemodynamic and metabolic balance is very sensitive, may go into hypothermia when blood and products stored at +4C⁰ are given without heating. In routine practice, blood transfusion is performed without heating. The concern here is that hemolysis may develop by heating the blood. Studies have shown that hemolysis occurs when blood is heated above 46C⁰. In this study, physiological heating is planned. In vitro neonatal experimental modeling has shown that there is no hemolysis with physiological heating. The aim of the researchers is; While protecting fragile, extremely premature babies from the complications of cold transfusion, the aim is to compare the transfusion groups with and without physiological heating in terms of hemolysis, metabolic balance and cerebral tissue oxygenation.


Clinical Trial Description

This trial is planned to be randomized and controlled. Erythrocyte transfusion (ET) will be applied to premature babies born below the 34th gestational week, based on the limit values specified by TND, during Level 3 routine intensive care treatment and follow-up. They will be divided into two groups of 20 babies each: control and study groups. The control group will receive erythrocyte transfusion without heating, which is routinely applied. Heated ET will be performed on the study group by physiological warming between 34-36C⁰. Procedures to be applied for the working group: 1. ET requirement will be determined in line with the TND guide. It will be transfused at a standard dose of 20 ml/kg. Before ET is performed, blood gas and HTC, K and blood temperature before entering the heater will be measured and recorded. 2. The erythrocyte suspension will be heated between 34-36 C⁰, which is the determined physiological temperature. 3. Before giving it to the baby, 2 ml of blood will be taken through a triple tap and its hematocrit and K value (blood gas) will be checked. It will be given to the baby after the temperature is checked with a body fluid thermometer and determined to be within the appropriate range and if hemolysis is not observed. 4. At the end of the standard transfusion period of 3 hours, all babies will be routinely checked for blood gases, HTC and K. As standard for all babies during transfusion; Heart rate, blood pressure, saturation and body temperatures will be monitored. It was planned to investigate whether there was a difference in terms of hypothermia and hemolysis between the groups with and without Physiological Heating. It will be examined whether heated blood has an effect on cerebral tissue perfusion by NIRS monitoring ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06425783
Study type Interventional
Source Goztepe Prof Dr Suleyman Yalcin City Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date April 1, 2024
Completion date March 2025

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04067973 - Impact of Prematurity on the Optic Nerve
Recruiting NCT05968586 - Non-Invasive Neurally Adjusted Ventilatory Assist (NAVA) Prone vs Supine in Premature Infants N/A
Not yet recruiting NCT05706584 - The Effect of Metaverse-Based Nursing Skills Laboratory N/A
Not yet recruiting NCT05530733 - Clinical Effects of Pacifier Use in Preterm During Orogastric Tube Feeding N/A
Withdrawn NCT04561700 - Nutritive Sucking Patterns in Premature Infants N/A
Recruiting NCT01443273 - Thrombophilic Risk Factors in Preterm and Infants Treated at Ha'Emek Medical Center Between the Years 1990 to 2010
Recruiting NCT04565210 - Effects of Oriental Music on Preterm Infants N/A
Not yet recruiting NCT06072625 - Enteral Feeding of Premature Babies and Olive Oil Supplementation N/A
Recruiting NCT04866342 - Servo Controlled Oxygen Targeting (SCO2T) Study: Masimo vs. Nellcor N/A
Enrolling by invitation NCT04168749 - Efficacy and Safety of Industrially Prepared 3 Chamber Bag Parenteral Nutrition for Premature Infant
Recruiting NCT04458441 - Can Warm Skin Disinfection Reduce the Pain Peripheral Central Catheter Application in Premature Babies? N/A
Recruiting NCT05835817 - Magnetoencephalography by Optical Pumping Magnetometer N/A
Enrolling by invitation NCT03061968 - Study of Applying Acupressure in Low-birth Weight Premature N/A
Recruiting NCT06207071 - Early DHA/ARA Supplementation in Growth-restricted Very Preterm Infants: A Randomized Clinical Trial N/A
Not yet recruiting NCT05806684 - Hyperbilirubinemia and Retinopathy of Prematurity in Preterm Infants: a Retrospective Study.
Recruiting NCT05380401 - Metabolic Mechanisms Induced by Enteral DHA and ARA Supplementation in Preterm Infants N/A
Completed NCT04298346 - Neurological Fate, Prematurity and Genetic Susceptibility Factors
Active, not recruiting NCT05343403 - Parental Participation on the Neonatal Ward - the neoPARTNER Study
Completed NCT04035564 - Early Sodium Intake in Preterm Newborns Phase 4
Recruiting NCT04432636 - Gut Bacteria and Brain of the Baby N/A