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Recruiting NCT07191678

NCT07191678 Mechanisms Affecting the Gut of Preterm Infants Receiving Blood Transfusion With Different Enteral Feed Interventions

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Clinical Trial Summary
NCT ID NCT07191678
Status Recruiting
Phase
Sponsor Imperial College Healthcare NHS Trust
Condition NEC - Necrotizing Enterocolitis
Study Type OBSERVATIONAL
Enrollment 270 participants
Start Date 2025-11-03
Primary Completion 2027-01-31

Eligibility & Interventions

Sex All sexes
Min Age 23 Weeks
Max Age 30 Weeks
Study Type OBSERVATIONAL

Eligibility Fast-Check

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What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 270 participants in total. It began in 2025-11-03 with a primary completion date of 2027-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

MAGPIE-2 is a prospective observational study designed to investigate the physiological mechanisms linking blood transfusion and enteral feeding practices to gut perfusion and oxygenation in very preterm infants. The study is nested within the WHEAT International randomised controlled trial, which compares two standard care approaches: withholding versus continuing milk feeds during red blood cell transfusion. While WHEAT evaluates clinical outcomes such as necrotising enterocolitis (NEC), MAGPIE-2 focuses on the underlying physiological changes that may contribute to NEC development. NEC is a serious gastrointestinal condition affecting approximately 10% of extremely preterm infants and is associated with high mortality and long-term neurodevelopmental impairment. Previous observational studies have suggested a temporal link between blood transfusion and NEC onset, particularly when feeds are continued during transfusion. However, the mechanisms remain poorly understood. MAGPIE-2 will use non-invasive monitoring tools-near-infrared spectroscopy (NIRS) and Doppler ultrasound-to measure cerebral and splanchnic (gut) tissue oxygenation and superior mesenteric artery (SMA) blood flow. These measurements will be used to calculate the Splanchnic-Cerebral Oxygenation Ratio (SCOR), a validated marker of gut tissue perfusion and ischaemia. A reduction in SCOR may indicate compromised gut oxygenation, potentially contributing to NEC. The study will recruit 270 infants (135 per arm) already enrolled in the WHEAT trial. Weekly measurements will be taken until 34 weeks corrected gestational age or discharge. Peri-transfusion monitoring includes continuous NIRS from 4 hours before to 4 hours after transfusion, and additional 2-hour recordings at approximately 24 and 48 hours post-transfusion. SMA Doppler assessments will be performed weekly. Primary outcomes include changes in SCOR post-transfusion between the two feeding strategies. Secondary outcomes include changes in cerebral and splanchnic oxygenation, SMA blood flow velocities, and the impact of severe anaemia (pre-transfusion haemoglobin ≤80 g/L) on these parameters. The study also includes an assessment of inter-operator variability in Doppler measurements. MAGPIE-2 aims to provide mechanistic insights that could inform safer transfusion and feeding practices in neonatal care, potentially reducing the incidence of NEC in this vulnerable population.

Eligibility Criteria

Inclusion Criteria: * Very preterm babies (born between 23 to \<30 weeks of gestational age ) in the WHEAT International trial * Written informed consent from parents Exclusion Criteria: * Babies who are deemed too unstable to perform the non-invasive monitoring and the ultrasound scan measurements by the attending clinical team * Babies who have already developed Bells stage 2 NEC, had bowel surgery or congenital abdominal conditions such as congenital diaphragmatic hernia, gastroschisis and exomphalos

Contact & Investigator

Central Contact

Jayanta Banerjee, MD (RES), FRCPCH, MBBS

✉ jayanta.banerjee@nhs.net

📞 07771826045

Frequently Asked Questions

Who can join the NCT07191678 clinical trial?

This trial is open to participants of all sexes, aged 23 Weeks or older, up to 30 Weeks, studying NEC - Necrotizing Enterocolitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07191678 currently recruiting?

Yes, NCT07191678 is actively recruiting participants. Contact the research team at jayanta.banerjee@nhs.net for enrollment information.

Where is the NCT07191678 trial being conducted?

This trial is being conducted at London, United Kingdom.

Who is sponsoring the NCT07191678 clinical trial?

NCT07191678 is sponsored by Imperial College Healthcare NHS Trust. The trial plans to enroll 270 participants.

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