Baking soda in epidural may reduce need for general anesthesia in urgent C-Sections
NCT ID NCT05313256
First seen Jun 27, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This study tested whether adding sodium bicarbonate (baking soda) to the standard epidural painkiller (lidocaine with epinephrine) could provide better pain relief for women needing an extremely urgent C-section during labor. 65 women were randomly assigned to receive either the buffered or standard version. The main goal was to see if fewer women would need general anesthesia due to inadequate pain control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine with epinephrine, with or without sodium bicarbonate (baking soda)
- What this could lead to
- If it works, this could offer faster, more reliable pain relief for emergency C-sections, lowering the need for general anesthesia.
- What could go wrong
- This is a small, completed Phase 2/3 trial with only 65 participants, so results may not apply widely. The intervention only targets pain during a specific procedure, not the underlying condition.
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 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
65 people
The number who actually took part.
- Started
-
Jul 2022
- Finished
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Jul 2024
- 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 years and older
- Sex
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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.
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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 patients, affiliated to social security * Informed consent signed by the participant and the investigating physician at the latest after the therapeutic intervention * Initial indication for vaginal delivery * Benefiting from emergency caesarean section during labour for fetal extraction with a maximum 15-minute decision-to-delivery delay (i.e. extremely urgent caesarean section) Exclusion Criteria: * Opposition to participation in research before delivery * Refusal or impossibility of informed consent * Lack of understanding or significant language barrier * Initial indication for general anaesthesia defined by the following situations: non-functional epidural analgesia, altered consciousness, eclampsia, suspicion of amniotic embolism, confirmed or suspected severe haemorrhage occurring before birth * Contraindication to the use of the products defined in the protocol : adrenalized lidocaine ; sodium bicarbonate. * Persons placed under judicial protection
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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
-
CH de la Côte Basque
Bayonne, France
-
CHU de Bordeaux
Bordeaux, France
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Other studies related to the condition(s) this trial covers.
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