C-section blood pressure drugs: which works best for baby?
NCT ID NCT06508359
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two drugs, norepinephrine and phenylephrine, to prevent or treat low blood pressure from spinal anesthesia during cesarean sections. 700 women having planned C-sections were randomly assigned to get the drug before blood pressure dropped (prophylactic) or only if it dropped (rescue). The main goal was to see how each approach affected the baby's umbilical cord blood pH, a measure of well-being at birth.
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 (vasopressors)
- What this could lead to
- If it works, this could help doctors choose the best timing and drug to prevent low blood pressure during C-sections, potentially improving newborn outcomes.
- What could go wrong
- This is a completed trial, but results may not apply to all patients or settings. The drugs themselves can cause side effects like fast or slow heart rate.
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
-
700 people
The number who actually took part.
- Started
-
Aug 2025
- Finished
-
Apr 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
-
18 to 45 years
- Sex
-
Female participants only
- Healthy volunteers
-
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: * 18-45 years * Primipara or multipara * Singleton pregnancy ≥37 weeks * American Society of Anesthesiologists physical status classification II * Scheduled for cesarean section under spinal anesthesia Exclusion Criteria: * Body height \< 150 cm * Body weight \> 100 kg or body mass index (BMI) ≥ 40 kg/m2 * Eclampsia or chronic hypertension or baseline blood pressure ≥140 mmHg * Hemoglobin \< 7g/dl * Fetal distress, or known fetal developmental anomaly
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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
-
General Hospital of Ningxia Medical University
Yinchuan, Ningxia, 750004, China
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