drugset / Trial / NCT07663149

Effectiveness of Continuous Phenylephrine in Preventing Shivering After Spinal Anesthesia in Cesarean Section

NCT07663149

Completed 108 enrolled Indonesia University
RandomizedParallel-groupOpen-labelPrevention

Summary

This study aims to evaluate the effectiveness of continuous phenylephrine infusion at 50 mcg/min in preventing shivering after spinal anesthesia in cesarean section. This study was an open-label randomized clinical trial involving patients undergoing cesarean section under spinal anesthesia. Subjects were allocated into two groups: without phenylephrine and continuous phenylephrine infusion at 50 mcg/min. The primary outcome was the incidence of shivering during observation, assessed using the Crossley and Mahajan scale. Secondary outcomes included hypotension, ephedrine requirement, hemodynamic adverse events, and nausea vomiting.

Timeline

Start
2026-04-07
Primary completion
2026-06-07
Completion
2026-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Phenylephrine Small molecule 50 ug Intravenous

Indications

No indication recorded.