Which drug best steadies blood pressure during C-Section in preeclampsia?
NCT ID NCT07795710
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This trial tests three medications, phenylephrine, norepinephrine, and ephedrine, to see which one best manages low blood pressure that can occur after spinal anesthesia in women with preeclampsia having a cesarean delivery. Researchers will give each participant one of the three drugs as needed and track heart rate and blood pressure changes. The goal is to find the safest and most effective option for this specific group of patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Three blood pressure medications: phenylephrine, norepinephrine, and ephedrine
- What this could lead to
- If one drug works best, it could guide safer blood pressure management during cesarean delivery for women with preeclampsia.
- What could go wrong
- The trial is small and early, and results may not apply to all patients. Each drug carries risks like heart rate changes or blood pressure swings.
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
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150 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Jan 2024
- 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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20 to 40 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.
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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: * Preeclamptic pregnant female * ASA II and III * singleton or twin pregnancies will be scheduled for caesarean delivery * diagnosis of preeclampsia as a new onset of hypertension and proteinuria. Exclusion Criteria: * chronic hypertension, labor or failed trial of labor, * body mass index ≥40 kg/m2 , * resting heart rate \<60 bpm, eclampsia, * known fetal anomalies, contraindications to spinal anesthesia, abruption placentae, and cord prolapas.
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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
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Minia University
Minya, Egypt
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Other studies related to the condition(s) this trial covers.
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