C-Section drug showdown: norepinephrine beats phenylephrine for stable blood pressure
NCT ID NCT07327320
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compared two medications, norepinephrine and phenylephrine, given continuously during C-sections to prevent dangerously low blood pressure. 98 women participated. Norepinephrine was more effective, causing low blood pressure in only 14.9% of cases compared to 42.6% with phenylephrine, and also led to steadier heart rates. Both drugs were safe for the babies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- norepinephrine and phenylephrine
- What this could lead to
- If confirmed, this could lead to a preferred drug for preventing low blood pressure during C-sections, improving safety and comfort for mothers.
- What could go wrong
- This is a single, small Phase 4 trial. Results may not apply to all hospitals or patients, and long-term effects were not studied.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
100 people
The number who actually took part.
- Started
-
Jun 2024
- Finished
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Oct 2025
- 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
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Accepted
You do not need to have the condition being studied to take part.
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: * Parturients aged ≥18 years * Classified as American Society of Anesthesiologists physical status II * Term singleton pregnancies * Scheduled for elective CD under SA Exclusion Criteria: * Refusal to participate. * Fetal anomalies or suspected fetal compromise * Preeclampsia or eclampsia * Conversion to general anesthesia or use of labor analgesia * Contraindication to SA * Preexisting cardiovascular or cerebrovascular disease; chronic hypertension * Baseline bradycardia * Current use of cardiovascular or antihypertensive medications * Body mass index more than 40 kg/m² * Body weight less than 50 kg or more than 100 kg
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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.
Contacts and locations
Locations
-
Tam Anh TP. Ho Chi Minh General Hospital
Ho Chi Minh City, Ho Chi Minh, 700000, Vietnam
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Other studies related to the condition(s) this trial covers.
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