drugset / Trial / NCT05133817
Prophylactic Norepinephrine Infusion Combined With Colloid Coloading for Postspinal Anesthesia Hypotension
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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.