Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 5:09 AM
Ignite Modification Date:
2025-12-25 @ 5:09 AM
NCT ID:
NCT07187427
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years
* Vaginal delivery
* Gestational age ≥ 37 weeks
* Requesting neuraxial analgesia
* French or English language
Exclusion Criteria:
* ASA score \> 3
* Allergy or contraindication to receiving opioids/local anesthesia (morphine or fentanyl)
* BMI \> 40 kg/m²
* Hepatic or renal failure,
* Severe preeclampsia and signs of severity according to the criteria of the American College of Obstetricians and Gynecologists
* Maternal hemorrhage (placental abruption, hepatic subcapsular hematoma,...)
* Severe scoliosis
* Biliary cholestasis or polymorphic eruption of pregnancy
* Inability to provide informed consent, either secondary to mental or physical disability or a significant language barrier (inability to understand English or French)
* Prior administration of an opioid or opioid misuse
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07187427
Study Brief:
Protocol Section:
NCT07187427