One dose before surgery: could a common steroid shield mothers from spinal Anesthesia's biggest risk?
NCT ID NCT07761585
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This trial tests whether a single intravenous dose of dexamethasone, given before spinal anesthesia, can prevent low blood pressure (spinal hypotension) in women having an elective cesarean section. Low blood pressure after spinal anesthesia is common and can cause nausea, dizziness, and reduced blood flow to the baby. Researchers will compare dexamethasone against a placebo, monitoring blood pressure during surgery and tracking the need for additional blood-pressure-raising medications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dexamethasone
- What this could lead to
- If effective, this simple pre-surgery dose could reduce a common complication of C-sections, improving safety and comfort for mothers and babies.
- What could go wrong
- This is a small, early-stage trial, and results may not apply broadly. Dexamethasone may not prevent hypotension, and any drug in pregnancy carries potential risks.
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
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
80 people
The number who actually took part.
- Started
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Feb 2026
- Finished
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Jul 2026
- Lead sponsor
-
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 years and older
- Sex
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Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pregnant females Consenting No contraindications Exclusion Criteria: * Non consenting
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Liaquat National Hospital
Karachi, Pakistan