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NOT YET RECRUITING
NCT07835529
NA

Magnesium Sulphate for Neonatal Asphyxia and Length of Hospital Stay

Sponsor: Sargodha Medical College

View on ClinicalTrials.gov

Summary

Neonatal asphyxia causes significant global morbidity, frequently resulting in Hypoxic-Ischemic Encephalopathy (HIE). In resource-limited settings where therapeutic hypothermia is unavailable, affordable neuroprotective options are needed. Intravenous magnesium sulphate blocks NMDA receptors, limiting cellular calcium influx and neuroinflammation. This randomized controlled trial evaluates whether adjuvant intravenous magnesium sulphate (250\\text{ mg/kg} within 6 hours of birth) reduces the duration of hospital stay and improves short-term clinical outcomes in term neonates with birth asphyxia.

Official title: Use of Magnesium Sulphate in Neonatal Asphyxia and Its Effect on Duration of Hospital Stay

Key Details

Gender

All

Age Range

Any - 24 Hours

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2026-11-01

Completion Date

2027-07-01

Last Updated

2026-09-23

Healthy Volunteers

No

Interventions

DRUG

Magnesium sulphate

Intravenous infusion of Magnesium Sulphate at a dose of 250\\text{ mg/kg} administered over 30\\text{--}60 minutes within 6 hours of birth

OTHER

Supportive care and standard neonatal intensive care unit care

Standard clinical supportive care including prompt resuscitation, maintenance of adequate ventilation, correction of metabolic abnormalities, and management of complications without Magnesium Sulphate.