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COMPLETED
NCT07663149
NA

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

Sponsor: Indonesia University

View on ClinicalTrials.gov

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.

Key Details

Gender

FEMALE

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

108

Start Date

2026-04-07

Completion Date

2026-06-07

Last Updated

2026-06-23

Healthy Volunteers

No

Interventions

DRUG

Phenylephrine

giving phenylephrine continous infusion at rate 50 mcg/minutes intravenously after insertion of spinal anesthesia

Locations (1)

RSUP dr. Cipto Mangunkusumo

Jakarta Pusat, Jakarta Special Capital Region, Indonesia