Actively Recruiting

Phase Not Applicable
Age: 37Weeks - 42Weeks
All Genders
NCT06540222

Sustained Cord Circulation at Emergency Cesarean Section

Led by Region Skane · Updated on 2025-09-22

2200

Participants Needed

12

Research Sites

320 weeks

Total Duration

On this page

Sponsors

R

Region Skane

Lead Sponsor

R

Region Stockholm

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Sustained Cord Circulation at Emergency Cesarean Section

Who Can Participate

Age: 37Weeks - 42Weeks
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Singleton neonate
  • Born alive
  • Gestational age 237 weeks
  • Born by emergency cesarean section with epidural or spinal anesthesia where pediatric/neonatal team is present
Not Eligible

You will not qualify if you...

  • Major congenital malformation affecting resuscitation or outcomes
  • Major genetic disorder affecting resuscitation or outcomes

AI-Screening

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Trial Site Locations

Total: 12 locations

1

Östra sjukhuset - Sahlgrenska Universitetssjukhuset

Gothenburg, Sweden

Actively Recruiting

2

Hallands sjukhus, Halmstad

Halmstad, Sweden

Actively Recruiting

3

Universitetssjukhuset i Linköping

Linköping, Sweden

Actively Recruiting

4

Skånes Universitetssjukhus

Lund, Sweden

Actively Recruiting

5

Skånes Universitetssjukhus, Malmö

Malmö, Sweden

Actively Recruiting

6

Universitetssjukhuset Örebro

Örebro, Sweden

Actively Recruiting

7

BB Stockholm

Stockholm, Sweden

Actively Recruiting

8

Danderyds sjukhus

Stockholm, Sweden

Actively Recruiting

9

Karolinska Universitetssjukhuset, Huddinge

Stockholm, Sweden

Actively Recruiting

10

Karolinska Universitetssjukhuset, Solna

Stockholm, Sweden

Actively Recruiting

11

Södersjukhuset - Sachsska barn- och ungdomssjukhuset

Stockholm, Sweden

Actively Recruiting

12

Norrlands universitetssjukhus

Umeå, Sweden

Actively Recruiting

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Research Team

O

Ola Andersson, MD PhD

CONTACT

J

Jenny Svedenkrans, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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