Obstetric Labor Complications Clinical Trial
— QETALOfficial title:
Alkalinization of Adrenalized Lidocaine in Extending Epidural Analgesia for Extremely Urgent Cesarean Section During Labor: a Randomized Controlled Trial.
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.
Status | Recruiting |
Enrollment | 66 |
Est. completion date | July 2024 |
Est. primary completion date | July 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
France | CH de la Côte Basque | Bayonne | |
France | CHU de Bordeaux | Bordeaux |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Resort to general anaesthesia | Resort to general anaesthesia for insufficient analgesia after epidural extension for extremely urgent caesarean section. | 15 minutes after inclusion | |
Secondary | Delay between fetal extraction decision and birth | Minutes between the decision to extract the fetus by the obstetrical team and the clamping of the umbilical cord | Between inclusion and birth | |
Secondary | Delay between fetal extraction decision and incision | Minutes between the decision to extract the fetus by the obstetrical team and the surgical incision | Between inclusion and cesarean section | |
Secondary | Maternal complications | Maternal complications after epidural top-up, including nausea-vomiting in the peroperative and postoperative period, desaturation episode, difficult orotracheal intubation, bronchial inhalation syndrome, hypotensive episode before fetal extraction, extended sensory or motor block. | up to 24 hours after inclusion | |
Secondary | Complementary medicines | Use and characterization of complementary medicines necessary for maternal well-being during caesarean section. | Between inclusion and cesarean section | |
Secondary | Postpartum hemorrhage | Postpartum hemorrhage (blood loss of more than 500 ml) | up to 24 hours after inclusion | |
Secondary | Paediatric wellness | Paediatric wellness criteria (umbilical cord pH less than 7.0 ; umbilical cord lactate) | at birth | |
Secondary | Anesthesia level | Anesthesia level one hour after surgical incision | one hour after surgical incision | |
Secondary | Maternal satisfaction | Maternal satisfaction regarding analgesia and anesthesia during caesarean section. | up to 4 hours after inclusion |
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