EICHORCondition: Obstetric Labor Complications · Sponsor: University Hospital, Bordeaux
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Prospective randomized study comparing the use of lidocaine 2% with epinephrine buffered with sodium bicarbonate and lidocaine 2% with epinephrine as epidural top-up for extremely urgent cesarean section during labour.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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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
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| CH de la Côte Basque | Bayonne, France | — |
| CHU de Bordeaux | Bordeaux, France | — |
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Source record: clinicaltrials.gov/study/NCT05313256