Leg lift test may predict blood pressure drops in C-Section patients
NCT ID NCT05133271
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tested whether a passive leg raising test, done before spinal anesthesia, can predict low blood pressure in women having planned C-sections. Researchers measured heart function with ultrasound before and after raising the legs. They then tracked blood pressure drops and the need for medication during surgery. The goal was to see if this simple test could identify women at higher risk.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors predict and prevent dangerous drops in blood pressure during C-sections, making the procedure safer.
- What could go wrong
- This is a small, completed observational study with only 64 participants. The test may not be accurate enough for routine use, and results may not apply to all patients.
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
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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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64 people
The number who actually took part.
- Started
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Feb 2021
- Finished
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Aug 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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18 years and older
- 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: * Adult women admitted to Necker Enfants Malades hospital for scheduled cesarean section under spinal anesthesia * Written informed consent Exclusion Criteria: * No health insurance * Urgent cesarean * Failure of spinal anesthesia * Free and informed consent impossible to obtain (especially due to a language barrier) * Severe cardiovascular or neurovascular comorbidities * Contraindication to the PLR (intracranial hypertension, fractures of the pelvis and / or lower limbs, ...) * Background of preeclampsia or eclampsia * Severe fetal pathology
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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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Hôpital Necker-Enfants Malades
Paris, 75015, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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