Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Completed NCT04245891

Neonatal Evaluation of Norepinephrine Infusion in Spinal Anesthesia for Cesarean Section

Conditions: Caesarean Section;Stillbirth

Sex: Female
Ages: 18 Years – N/A
Enrollment: 265
Sponsor: Centre Hospitalier Universitaire de Nīmes

Location: CHU de Nîmes Nîmes Gard

Summary

This retrospective study aims to evaluate the fate of children born by cesarean section under spinal anesthesia with or without norepinephrine as vasopressor support for anesthesia. The main objective is to compare the initial Apgar score. The records of patients who received norepinephrine are compared to those without norepinephrine. To limit the biases of this type of study, the investigators will apply a propensity score that will include as a variable: age, ASA score, comorbidity, urgency. The patients analysed correspond to the period 2016-2017.

Eligibility Criteria

Inclusion Criteria: * age \> 18 * Spinal Anesthesia for Cesarean Section Exclusion Criteria: * sub epidural cesarean section * contraindication to spinal anesthesia (allergy, severe heart disease, coagulopathy)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04245891). StuddyBuddy aggregates publicly available trial information.