Ultrasound may improve spinal anesthesia success in obese Moms-to-Be
NCT ID NCT07549776
First seen Jun 26, 2026 · Last updated Jul 08, 2026 · Updated 3 times
Summary
This study compared two ways to find the right spot for spinal anesthesia in 100 obese women having C-sections. One group used ultrasound to guide the needle, the other used traditional touch-based landmarks. The goal was to see which method leads to a successful first attempt, reducing pain and complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ultrasound-guided preprocedural marking
- What this could lead to
- If ultrasound proves better, it could make spinal anesthesia faster and less painful for obese women undergoing C-sections.
- What could go wrong
- This is a small, completed trial with 100 participants, so results may not apply to all hospitals or patients. Ultrasound requires extra training and equipment.
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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100 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Jan 2026
- 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: * Age ≥ 18 years * Pregnant women undergoing cesarean section * Body mass index (BMI) ≥ 30 kg/m² at the time of cesarean section * Scheduled for cesarean section under spinal anesthesia Exclusion Criteria: * Congenital spinal deformities * History of spinal surgery * Coagulopathy * Infection at the puncture site * Allergy to local anesthetics * Emergency cesarean section (NICE category 1)
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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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National Maternal and Perinatal Institute
Lima, Lima Province, 15001, Peru
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