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Clinical Trial Summary

To compare two infusion rates of norepinephrine for prophylaxis against post-spinal hypotension during caesarean delivery.


Clinical Trial Description

Hypotension after spinal anesthesia for cesarean delivery is common and is caused mainly by peripheral vasodilatation. Although the intravenous administration of fluids helps, it does not always prevent maternal hypotension. Usually, this hypotension is treated with phenylephrine or ephedrine. Norepinephrine has been recently introduced for prophylaxis against post-spinal hypotension during cesarean delivery due to its α-adrenergic activity in addition to the weak β-adrenergic activity. Although the use of norepinephrine for this purpose has shown promising results. However, no sufficient data are available with regard to its optimum dose. The objective of this study is to compare two infusion rates of norepinephrine for prophylaxis against post-spinal hypotension during caesarean delivery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06102382
Study type Interventional
Source Assiut University
Contact Zakaria A. Zakaria
Phone +201150637566
Email za6841924@gmail.com
Status Not yet recruiting
Phase N/A
Start date December 10, 2023
Completion date December 10, 2024

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