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Study identifier: NCT06540222 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Sustained Cord Circulation at Emergency Cesarean Section

Condition: Asphyxia Neonatorum · Fetal Hypoxia  ·  Sponsor: Region Skane

PhaseNA
Planned participants2200
Who can joinAll sexes, 37 Weeks to 42 Weeks
Healthy volunteersNo

About this study

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 provides better outcomes. Participants (term neonates born by emergency Cesarean section) will: Receive resuscitation with either sustained cord circulation or standard care Be monitored for admission to neonatal care and other predefined health outcomes

This description comes directly from the study's public registry record.

Talk to the study team

Ola Andersson, MD PhD  ·  ‭+46 70-966 41 80  ·  ola.andersson@med.lu.se

Jenny Svedenkrans, MD PhD  ·  ‭+46 72-469 86 60  ·  jenny.svedenkrans@ki.se

Always discuss trial participation with your own doctor first.

Locations (12)

Östra sjukhuset - Sahlgrenska UniversitetssjukhusetGothenburg, SwedenRecruiting
Hallands sjukhus, HalmstadHalmstad, SwedenRecruiting
Universitetssjukhuset i LinköpingLinköping, SwedenRecruiting
Skånes UniversitetssjukhusLund, SwedenRecruiting
Skånes Universitetssjukhus, MalmöMalmö, SwedenRecruiting
Universitetssjukhuset ÖrebroÖrebro, SwedenRecruiting
BB StockholmStockholm, SwedenRecruiting
Danderyds sjukhusStockholm, SwedenRecruiting
Karolinska Universitetssjukhuset, HuddingeStockholm, SwedenRecruiting
Karolinska Universitetssjukhuset, SolnaStockholm, SwedenRecruiting
Södersjukhuset - Sachsska barn- och ungdomssjukhusetStockholm, SwedenRecruiting
Norrlands universitetssjukhusUmeå, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT06540222