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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04245891
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase
Start date May 1, 2016
Completion date November 30, 2017

See also
  Status Clinical Trial Phase
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Not yet recruiting NCT03154866 - Lactobacillus Kefiri LKF01 (DSM32079) in Newborns Born by Caesarian Section Phase 4