Sustained Cord Circulation at Emergency Cesarean Section
Recruiting
N/A
Interventional Study
Asphyxia Neonatorum
Fetal Hypoxia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 37 Weeks – 42 Weeks
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 2,200 (estimated)
- Sponsor
- Region Skane · Other
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About This Trial
The goal of this clinical trial is to evaluate if sustained cord circulation during resuscitation improves outcomes for term neonates born by emergency Cesarean section. The main question it aims to answer is: Does sustained cord circulation reduce admission rates to neonatal care?
Researchers will compare resuscitation with an uncut umblical cord to standard resuscitation practices to see if it …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Singleton neonate
* Born alive
* Gestational age ≥37 weeks
* Born by emergency cesarean section, epidural/spinal anesthesia, where the pediatric/neonatal team has been called for to attend.
Exclusion Criteria:
* Major congenital malformation that may affect resuscitation or …
Contacts