MAGNESIUM SHOT BEFORE PRETERM BIRTH MAY PREVENT CEREBRAL PALSY
NCT ID NCT07524972
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether giving magnesium sulphate to pregnant women at high risk of preterm birth can protect their babies from cerebral palsy. About 138 women between 32 and 35 weeks of pregnancy will receive either magnesium or a placebo before delivery. Researchers will then track the babies' brain development to see if the treatment reduces the risk of death or cerebral palsy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- magnesium sulphate
- What this could lead to
- If it works, this could offer a simple, low-cost way to prevent cerebral palsy in babies born early.
- What could go wrong
- This is a single-center trial with 138 participants, so results may not apply broadly. Magnesium sulphate can cause side effects like flushing or low blood pressure in mothers.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 138 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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May 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* Inclusion Criteria: * Pregnant women at high risk of preterm birth between 32 and 35 weeks of gestation * Birth is planned or expected within 24 hours * Singleton pregnancy * No contraindication to antenatal magnesium sulphate * Able to provide informed consent * Exclusion Criteria: * Higher-order multiple pregnancy * Received antenatal magnesium sulphate during the current pregnancy for hypertension or preeclampsia * Magnesium sulphate is required for treatment of preeclampsia * Second stage of labor * Respiratory rate less than 16 breaths per minute * Absent patellar reflexes * Urine output less than 100 mL in the previous 4 hours * Renal failure * Hypocalcemia * Myasthenia gravis * Magnesium sulphate infusion had to be stopped because of adverse effects
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Suez Canal University
RECRUITINGIsmailia, Ismailia Governorate, 8366004, Egypt
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