Management Arterial Hypotension During Planned Caesarean Section,

Status Recruiting

Clinical Trial Summary

Comparison of two practices of obstetrical services between the CHU of Clermont Ferrand and the HFME Lyon-Bron in the management of arterial hypotension during an elective cesarean section

Clinical Trial Description

The investigators propose to carry out a bicentric strict observational prospective study between the maternity of the HFME of Lyon-Bron which uses the mixture ephedrine / noradrenaline with the PSE for many years in service protocol for the management of hypotension for cesarean section under perimedullary anesthesia and the CHU of Clermont-Ferrand which uses baby noradrenaline 10 mcg/mL PSE for this same indication according to an institutional protocol. Patients corresponding to the inclusion and non-inclusion criteria will be recruited by a physician investigator and will give their agreement of non-opposition after having received clear oral and written information about our study. The care will not be modified in any way compared to the usual practices of the service. ;

Study Design

Related Conditions & MeSH terms

Hypotension

Clinical Trial Details

NCT number	NCT05513066
Study type	Observational
Source	University Hospital, Clermont-Ferrand
Contact	Lise Laclautre
Phone	334.73.754.963
Email	promo_interne_drci@chu-clermontferrand.fr
Status	Recruiting
Phase
Start date	September 2, 2022
Completion date	February 1, 2024

View Details

See also
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Management Arterial Hypotension During Planned Caesarean Section, Intravenous Ephedrine/Phenylephrine Mixture Versus Intravenous Baby Noradrenaline — ARTEMIS

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms