New spinal technique may prevent blood pressure drops during C-Sections
NCT ID NCT07327866
First seen Jan 11, 2026 · Last updated Jun 23, 2026 · Updated 28 times
Summary
This study compares two ways of giving spinal anesthesia for planned C-sections: the standard single injection versus a sequential (two-part) injection. The goal is to see if the sequential method reduces the chance of a sudden drop in blood pressure, a common and risky side effect. About 94 women aged 18-45 will take part, and their blood pressure will be monitored closely after the injection.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Al-Azhar University
Cairo, Egypt, 11865, Egypt
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
bupivacaine and fentanyl (spinal anesthetic)
What this could lead to
If it works, this could lead to a safer spinal anesthesia technique for C-sections, reducing the risk of dangerous blood pressure drops.
What could go wrong
This is a small, early-phase trial with only 94 participants, so results may not apply to all patients. The sequential method may also be more complex to perform.
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.