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Extrauterine Placental Transfusion In Neonatal Resuscitation Of Very Low Birth Weight Infants

Extrauterine Placental Transfusion In Neonatal Resuscitation (EXPLAIN) of Very Low Birth Weight Infants (VLBW): A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03916159
Acronym
EXPLAIN
Enrollment
60
Registered
2019-04-16
Start date
2019-05-01
Completion date
2023-10-24
Last updated
2023-11-08

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

Conditions

Anemia, Placental Transfusion, Very Low Birth Weight Infant

Keywords

extrauterine placental transfusion, delayed cord clamping, neonatal resuscitation

Brief summary

To investigate the effect of extrauterine placental transfusion (EPT) compared to delayed cord clamping (DCC) on the mean hematokrit on the first day of life in very low birth weight infants (VLBW) born by caesarian section. The investigators hypothesize that EPT provides higher blood volume during neonatal transition and improves neonatal outcome of VLBW infants.

Detailed description

This prospective randomized controlled study will be conducted among 2 groups, all of them are preterm infants with birth weight less than 1500 g (very low birth weight (VLBW)) who are delivered by caesarean section, in the first interventional group an extrauterine placental transfusion (EPT) will be done during neonatal resuscitation with respiratory pressure support. There will be a delayed cord clamping (DCC) of at least 30 - 60 seconds in the control group, before starting neonatal resuscitation with respiratory support. In EPT approach preterm born infants are delivered by caesarean section with the placenta still attached to the infant via the umbilical cord. Then, placental transfusion is performed up to several minutes by holding the placenta \ 40-50cm above the babies' heart level while respiratory support by mask continuous-positive-airway-pressure (CPAP) is initiated simultaneously. Extrauterine placental transfusion may give more blood in babies delivered by cesarean section and may improve perfusion during the fetal-to-neonatal transition with impact on neonatal outcome.

Interventions

PROCEDUREExtrauterine placental transfusion (Intervention group)

At delivery by caesarean section, the infant is born with the placenta still attached via the umbilical cord and placental transfusion is performed at least 1 minute but not more than 10 minutes by holding the placenta \ 40-50cm above the babies' heart level while respiratory support by mask continuous-positive-airway-pressure (CPAP) is initiated simultaneously.

PROCEDUREDelayed cord clamping (Control group)

At delivery by caesarean section, delayed cord clamping will be performed by having the delivering obstetrician delay clamping of the umbilical cord for at least 30 seconds with initiation of respiratory support by mask CPAP after cord clamping.

Sponsors

Universitätsklinikum Köln
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
24 Weeks to No maximum
Healthy volunteers
No

Inclusion criteria

* Birth weight \< 1500 gram (very low birth weight infant) * Delivery by caesarean section * Gestational age \> 23+6 weeks

Exclusion criteria

* Vaginal delivery * Fetal or maternal risk (i.e. compromise, emergency c-section) * Congenital anomalies and/or major cardiac defects * Placental abruption or previa with hemorrhage * Placenta accreta or increta * Monochorionic multiples (i.e. Di/Mo or Mo/Mo twins) * Parents declined study

Design outcomes

Primary

MeasureTime frameDescription
Hematocrit0 - 24 hours of lifeMean Hematocrit in the first 24 hours of life

Secondary

MeasureTime frameDescription
Mean airway pressureDuring first hour of lifeMean airway pressure given in cmH2O during neonatal resuscitation
Mean tidal volumeDuring first hour of lifeMean tidal volume given in milliliter (ml) during neonatal resuscitation
Heart rateDuring first hour of lifeHeart rate given in beats-per-minute (bpm) during neonatal resuscitation
Blood oxygen saturationDuring first hour of lifeTranscutaneous measured blood oxygen saturation given in percent (%) during neonatal resuscitation
Admission temperatureAdmission to ward is up to 120 minutes of ageMean temperature at admission
All Grade Intraventricular Hemorrhage (IVH)Up to 28 days of lifeIncidence of any intraventricular hemorrhage (grades 1-4)
All Grade BPDAt the corrected age of 36 weeksIncidence of Bronchopulmonary Disease (BPD) (all grades)
Spontaneous Pneumothorax/PneumoperitoneumDuring the first 7 days of lifeEarly incidence of spontaneous pneumothorax and/or pneumoperitoneum
Cerebral tissue oxygen saturationDuring first hour of lifeTranscutaneous measured cerebral tissue oxygen saturation given in percent (%) during neonatal resuscitation
Retinopathy of Prematurity (ROP), higher gradesAt the corrected age of 40 weeksIncidence of retinopathy of prematurity with treatment (drugs and/or surgery)
DeathUntil corrected age of 40 weeksIncidence of death in studied infants
Number of participants who received red blood cell (RBC) transfusionDuring the first 7 days of lifeAmount of RBC Transfusion \[cumulative ml/kg over the first 7 days\] in those participants who received RBC transfusion
HyperbilirubinemiaDuring the first 14 days of lifePeak bilirubin concentration
Blood Exchange TransfusionDuring the first 14 days of lifeIncidence of blood exchange transfusion due to critical hyperbilirubinemia of the neonate.
Intubation and Mechanical VentilationDuring the first 72 hours of lifeIncidence of intubation and time duration of mechanical ventilation
Neurodevelopmental Outcome22-26 month corrected gestational ageBayley Scales of Infant and Toddler Development - Third Edition (Bayley-III) composite score (motor, cognitive, language)
NEC/SIP with surgeryDuring the first 28 days of lifeIncidence of necrotizing enterocolitis (NEC) and/or spontaneous intestinal perforation (SIP) with need for surgery

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026