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:
2025-12-26 @ 2:39 PM
Ignite Modification Date:
2025-12-26 @ 2:39 PM
NCT ID:
NCT04946006
Eligibility Criteria:
Inclusion Criteria:
* Elective uncomplicated cesarean delivery under neuraxial anesthesia
* \>18 year-old with ASA status II or III, with a singleton gestation and a gestational age between 37 to 42 weeks Informed consent to participate in this study
Exclusion Criteria:
* Refusal to give written informed consent
* Allergy or hypersensitivity to oxytocin
* Body mass index ≥ 40 kg/m2on the day of admission
* A history of hypertension and/ or severe cardiac disease(s)
* Contra-indications for neuraxial anesthesia
* Conditions that predispose to uterine atony and postpartum hemorrhage such as placenta previa, multiple gestation, preeclampsia, macrosomia (≥ 4 kg), polyhydramnios, uterine fibroids in and near operating field, previous history of uterine atony and postpartum bleeding, or bleeding diathesis.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT04946006
Study Brief:
Protocol Section:
NCT04946006