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:
2025-12-24 @ 10:51 PM
Ignite Modification Date:
2025-12-24 @ 10:51 PM
NCT ID:
NCT01865669
Eligibility Criteria:
Inclusion Criteria:
* patients who give written informed consent
* patients requiring elective primary or 1st repeat Cesarean section
* patients with gestational age 37-41 weeks
* non-labouring patients, not exposed to exogenous oxytocin
* Cesarean section under spinal anesthetic
* patients \<30 years of age with a normal pre-pregnancy BMI (20 and 24.9 kg/m2)
* patients ≥40 years of age with a normal pre-pregnancy BMI
* patients with a BMI≥40 kg/m2 and age \<30 years
Exclusion Criteria:
* patients who refuse to give written informed consent
* patients who require general anesthesia
* patients who have had more than one previous uterine surgery/CS
* patients with placental abnormalities (abruption, accreta, percreta)
* patients with bleeding disorders
* presence of any other risk factors for PPH
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT01865669
Study Brief:
Protocol Section:
NCT01865669