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Study identifier: NCT07524972 Synced from ClinicalTrials.gov · July 28, 2026
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Antenatal Magnesium Sulphate in High-Risk Preterm Patients

Condition: Cerebral Palsy · Magnesium Sulfate Overdose  ·  Sponsor: Cairo University

PhasePhase 3
Planned participants138
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to evaluate whether antenatal magnesium sulphate reduces the risk of cerebral palsy in infants born to women at high risk of preterm birth. It will also assess the safety of magnesium sulfate for both the mother and the neonate. The main question it aims to answer is whether magnesium sulphate given before anticipated preterm delivery decreases the incidence of cerebral palsy without causing significant maternal or neonatal adverse effects. Researchers will compare magnesium sulphate with a placebo in women at high risk of preterm birth between 32 and 35 weeks of gestation. Participants will be randomly assigned to receive either intravenous magnesium sulphate or a placebo before delivery, and maternal and neonatal outcomes will be followed after birth, including neurodevelopmental assessment of the infant.

This description comes directly from the study's public registry record.

Talk to the study team

mohamed shaaban, MD  ·  +2010 05153911  ·  mshaaban@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Suez Canal UniversityIsmailia, Ismailia Governorate, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07524972