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Clinical Trials/NCT06264284
NCT06264284
Completed
N/A

Emergency (Red Code) Cesarean Section : Maternal and Fetal Prognosis Depending on Anesthetic Modalities in a Level 3 Maternity Ward

Central Hospital, Nancy, France1 site in 1 country150 target enrollmentJuly 19, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Anesthesia Complication
Sponsor
Central Hospital, Nancy, France
Enrollment
150
Locations
1
Primary Endpoint
To evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

We try to evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome on emergency (Red Code) Cesarean Section.

This study occurred in a Level 3 Maternity Ward.

Registry
clinicaltrials.gov
Start Date
July 19, 2018
End Date
July 19, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Central Hospital, Nancy, France
Responsible Party
Principal Investigator
Principal Investigator

STANOWSKI Mattieu

MD

Central Hospital, Nancy, France

Eligibility Criteria

Inclusion Criteria

  • Pregnant women
  • emergency "code red" cesarean section

Exclusion Criteria

  • Any other intervention
  • Planned cesarean section

Outcomes

Primary Outcomes

To evaluate whether the type of anesthesia used influences the occurrence of perioperative maternal complications as well as neonatal outcome

Time Frame: From July 19, 2018 to July 19, 2023.

Identify all pregnant women who received an emergency "code red" cesarean section Confront epidural anesthesia and general anesthesia on maternal complications (low blood pressure, anesthetic failure) and neonatal outcomes (Apgar scores, arterial pH at the umbilical cord, arterial lactate, need for tracheal intubation at birth, admission of the newborn to intensive care/intensive care, death)

Study Sites (1)

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