drugset / Trial / NCT05133817

Prophylactic Norepinephrine Infusion Combined With Colloid Coloading for Postspinal Anesthesia Hypotension

NCT05133817

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate the suitable infusion dose of prophylactic norepinephrine infusion combined with 6% Hydroxyethyl starch (130/0.4) coload for post-spinal anesthesia hypotension in patients undergoing cesarean section.

Timeline

Start
2021-11-26
Primary completion
2022-09-03
Completion
2022-09-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Norepinephrine Other / unclassified 0.025 ug/kg Intravenous
Subject Norepinephrine Other / unclassified 0.05 ug/kg Intravenous
Subject Norepinephrine Other / unclassified 0.075 ug/kg Intravenous
Subject Norepinephrine Other / unclassified 0.1 ug/kg Intravenous

Indications

No indication recorded.