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Intact-cord Stabilisation and Physiology-based Cord Clamping in Caesarean Sections

Feasibility-testing of Extra-uterine Placental Transfusion to Facilitate Intact-cord Stabilisation and Physiology-based Cord Clamping for Term and Preterm Infants Delivered by Acute or Planned Caesarean Section

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05461950
Acronym
INTACT
Enrollment
263
Registered
2022-07-18
Start date
2022-10-03
Completion date
2024-03-31
Last updated
2024-06-04

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

Conditions

Cesarean Section, Infant Conditions

Keywords

infant stabilisation, intact umbilical cord, umbilical cord clamping, placental transfusion, cesarean section

Brief summary

This is a feasibility study with historical control designed to evaluate whether delivery of the placenta prior to umbilical cord clamping at caesarean sections is a feasible, safe and acceptable way of facilitating intact-cord stabilisation of preterm and term newborn infants.

Detailed description

Standard procedure when an infant is delivered by caesarean section is to wait to clamp the umbilical cord for approximately one minute, and then transfer the infant to a designated area for assessment and stabilisation. If the infant needs immediate resuscitation, the umbilical cord is cut earlier to expedite transfer to resuscitation equipment and qualified care (including stimulation, clearing airways and respiratory support). It has been suggested in several pilot and clinical studies that keeping the umbilical cord intact during the infant's transition from intra- to extrauterine life may improve outcomes and survival, especially for preterm infants. Since length of the umbilical cord is limited, finding ways to avoid cutting the cord while initiating stabilisation and care is warranted. To date, most studies have reported on interventions that involve mobile resuscitation equipment; thus keeping the infant in close proximity to the mother. This may be extra challenging in caesareans sections, especially due to space constraints and maintenance of sterility. The objective of this study to determine whether extra-uterine placental transfusion to facilitate intact-cord stabilisation and physiology-based cord clamping for infants delivered by caesarean section is feasible, safe and acceptable for infants and their mothers, as well as for involved personnel.

Interventions

PROCEDUREExtrauterine placental transfusion and physiology-based umbilical cord clamping

Placenta is delivered prior to umbilical cord clamping to facilitate placental transfusion. Infant and placenta are transferred to a warmer in an adjacent room, the umbilical cord is clamped and cut when the cord is white, pulsations have ceased and the infants is breathing regularly (within 10 minutes after delivery)

PROCEDUREExtrauterine placental transfusion, intact cord stabilisation and physiology-based umbilical cord clamping

Placenta is delivered prior to umbilical cord clamping to facilitate placental transfusion. Infant and placenta are transferred to a warmer in an adjacent room and necessary respiratory support is initiated (CPAP or PPV) by a neonatal team. The umbilical cord is clamped and cut when the cord is white, pulsations have ceased and the infant is breathing regularly with or without support (at maximum 10 minutes after delivery)

Umbilical cord is clamped and cut minimum 60 seconds after delivery to facilitate placental transfusion. Placenta is delivered after cord clamping. Infants needing respiratory support or other stabilisation are transferred to a warmer in the adjacent room where a neonatal team is waiting.

Sponsors

Norwegian University of Science and Technology
CollaboratorOTHER
Helse Møre og Romsdal HF
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
32 Weeks to 42 Weeks
Healthy volunteers
No

Inclusion criteria

* live infants (singletons or dichorionic twins) born in gestational week 32+0 to 42+0 * delivered by CS in regional anaesthesia * immediate care may be planned with involved personnel prior to delivery * informed maternal consent is obtained (parental consent on behalf of the unborn child).

Exclusion criteria

* twins, triplets * significant congenital malformations * placenta complications with high risk of abnormal maternal blood loss * severe fetal distress requiring cesarean section in general anaesthesia (crash CS) * participation in any other clinical study within the last month * not sufficient time for preparations or collection of maternal/parental consent * mother does not comprehend Norwegian or English

Design outcomes

Primary

MeasureTime frameDescription
Intervention fidelity (cohort 1)First 10 minutes after deliveryExtra-uterine placental transfusion + physiology-based cord clamping applied (for vigorous infants), measured as proportion of completed checklists. Registered by staff, using checklists in the operating room.
Intervention fidelity (cohort 2)First 10 minutes after deliveryExtra-uterine placental transfusion + intact-cord stabilisation + physiology-based cord clamping applied (for infants needing any respiratory support), measured as proportion of completed checklists. Registered by staff, using checklists in the operating room.

Secondary

MeasureTime frameDescription
Umbilical cord blood samples (cohort 1+2)Within 40-60 seconds after birthTime from birth to sampling for umbilical cord blood gas analysis (arterial and venous) completed (measured in seconds). Registered on a checklist by a time-keeper in the operating room.
Delivery of placenta (cohort 1+2)At 1 minute (+/- 10 seconds) after birthTime from birth to delivery of the placenta (measured in minutes ans seconds), registered on checklist by a time-keeper in the operating room
Respiratory support (cohort 2)First 10-15 minutes after birthType of respiratory support applied. Alternatives are: CPAP (Continuous Positive Airway Pressure) or PPV (Positive Pressure Ventilation) Registered on a special data collection sheet by the attending neonatal team or midwife
Duration of respiratory support (cohort 2)First 10-15 minutes after birthDuration of respiratory support (CPAP or PPV), measured in minutes and seconds. Registered on a special data collection sheet by the attending neonatal team or midwife
Apgar scoreAt 5 minutes after birth (cohort 1+2)Composite of heart rate, breathing effort, skin colour, muscle tone and reflexes (each sub scale 0 (absent), 1, 2 (normal). Minimum 0, maximum 10. Assessed and registered on a special data collection sheet by the attending midwife or neonatal nurse
Stabilisation (cohort 2)Within 10-20 minutes after birthTime from birth to stabilisation achieved (regular breathing, heartrate (HR) \>100, Saturation (SpO2) \>85%, inspired oxygen fraction (FiO2) \<40%. Measured in minutes and seconds. Assessed and registered on a special data collection sheet by the attending midwife or neonatal nurse
Cord clamping time (cohort 1+2)Within 10 minutes after birthTime from birth to umbilical cord clamping (measured in minutes and seconds), registered on a special data collection sheet by the attending midwife
Skin-to-skin-contact (cohort 1+2)Within 2 hours after birthTime from birth to continuous skin-to-skin contact between infant and mother (or other parent), measured in minutes. Registered on a checklist by the attending midwife or neonatal nurse
Residual placenta volume (cohort 1+2)Within 10-15 minutes after birthDrained and weighed residual blood volume from placenta and umbilical cord after cord clamping (measured in grams, converted to milliliters by a ratio of 1.05:1). Registered by the attending midwife or assistant nurse
Dry-electrode ECG attached (cohort 1+2)Within 10 seconds after birthTime from birth to dry-electrode ECG (NeoBeat) is attached to the infant's chest or abdomen (measured in seconds). Registered on a checklist by a time-keeper in the operating room.
First cry or breathing effort (cohort 1+2)Within 10 minutes after birthTime from birth to infant's first cry or attempt of spontaneous breathing (measured in minutes and seconds). Assessed by attending midwife or pediatric registrar. Registered on a checklist by a time-keeper in the operating room.
Heart rate (cohort 1+2)First 10 -15 minutes after birthInfant's heart rate after birth measured by a dry-electrode ECG (NeoBeat). Registered on a special data collection sheet by a timekeeper or attending midwife. Data are transferred wirelessly from the NeoBeat device to the Liveborn App (installed on a designated tablet) for storage and further analysis.
Apgar score (cohort 1+2)At 1 minute after birthComposite of heart rate, breathing effort, skin colour, muscle tone and reflexes (each sub scale 0 (absent), 1, 2 (normal). Minimum 0, maximum 10. Assessed by the attending midwife or pediatric registrar, registered on a special data collection sheet by a timekeeper in the operating room

Other

MeasureTime frameDescription
Post-operative maternal HemoglobinWithin 24 hours after cesarean sectionMaternal Hemoglobin value from a venous blood sample taken after cesarean section, measured in grams per 100 ml. Registered on a checklist and in the patient's record by the midwife
Low Apgar score (all cohorts)At 5 minutes after birthPrevalence of infant Apgar score less than 7 (mild asphyxia), composite of heart rate, breathing effort, skin colour, muscle tone and reflexes (subscale range from 0-2). Assessed and registered on a special data collection sheet and in the patient's record by the attending midwife or neonatal team
Infant hypothermia (all cohorts)Within 2 hours after birthPrevalence of infant rectal temperature less than 36.5 degrees celsius, measured by a thermometer and registered on a special data collection form and in the patient's record by the attending midwife or neonatal team
Admittance to Neonatal Intensive Care Unit (NICU) (all cohorts)Within 24 hours after birthIndication for infant's admittance to neonatal intensive care unit after birth. Assessed by the attending pediatric registrar or neonatologist. Registered in a special data collection sheet and in the patient's record
Days in NICU (all cohorts)Maximum 2 monthsInfant's length of stay i neonatal intensive care unit, measured in days. Registered on a checklist and in the patient's record by the neonatal team
Post-cesarean infection (all cohorts)Within14 days after surgery (cesarean section)Prevalence of maternal post-operative wound infection needing antibiotic therapy. Registered in a dedicated paper form in the patient's record by the attending obstetrician
Abnormal blood loss (all cohorts)45 minutes from incision timePrevalence of abnormal maternal blood-loss during surgery and wound closure (more than 1000 ml). Estimated by staff by visual inspection and count of blood-soaked compresses. Registered in the patient's record by the attending obstetrician
Pre-operative maternal HemoglobinWithin 48 hours before cesarean sectionMaternal Hemoglobin value from a venous blood sample taken before cesarean section, measured in grams per 100 ml. Registered on a checklist and in the patient's record by the midwife

Countries

Norway

Outcome results

None listed

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