Comparaison of 3 Protocols of Ocytocin Administration in C Section

Status Completed

Clinical Trial Summary

Clinical Trial Description

This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturients during elective or urgent C section under spinal anesthesia.

The aim was to determine the lowest efficient dose to prevent post partum hemorrage and with the lowest incidence of maternal side effects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04046510
Study type	Interventional
Source	Mongi Slim Hospital
Contact
Status	Completed
Phase	N/A
Start date	September 1, 2018
Completion date	July 31, 2019

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