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NOT YET RECRUITING
NCT07913828
PHASE4

Two Doses of IV Magnesium Sulfate for Prevention of Post-Spinal Shivering

Sponsor: Suez Canal University

View on ClinicalTrials.gov

Summary

The main purpose of the study is to compare the incidence of clinically significant shivering, defined as Grade 3 or 4 on the Crossley-Mahajan shivering scale, within 60 minutes after spinal anesthesia. The study will also compare the severity and onset of shivering, the need for rescue treatment with intravenous pethidine, blood pressure, heart rate, body temperature, sedation, maternal adverse effects, and neonatal outcomes including Apgar scores, need for respiratory support, and admission to the neonatal intensive care unit.

Official title: Comparison Between Two Different Doses of Intravenous Magnesium Sulfate for Prevention of Post-Spinal Shivering During Cesarean Section: A Double-Blind Randomized Clinical Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

82

Start Date

2026-11-02

Completion Date

2026-12-15

Last Updated

2026-11-03

Healthy Volunteers

No

Interventions

DRUG

Magnesium Sulfate 50 mg/kg IV

Magnesium sulfate 50 mg/kg was diluted in 100 mL of normal saline and administered intravenously using an infusion pump over 20 minutes, starting immediately after spinal anesthesia.

DRUG

Magnesium Sulfate 30 mg/kg IV

Magnesium sulfate 30 mg/kg was diluted in 100 mL of normal saline and administered intravenously using an infusion pump over 20 minutes, starting immediately after spinal anesthesia.

Locations (1)

Suez Canal University Hospitals

Ismailia, Ismailia Governorate, Egypt