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 @ 1:55 PM
Ignite Modification Date:
2025-12-24 @ 1:55 PM
NCT ID:
NCT06761495
Eligibility Criteria:
Inclusion criteria:
* Pregnant women undergoing C/S for the first time
* 37 weeks \< gestation (term pregnancies)
Exclusion Criteria:
* Presence of regular contractions in the uterus
* Cervical dilatation of more than 4 cm, indicating the onset of the active phase of labour
* Placental abnormalities
* Previous uterine surgery
* Multiple pregnancy
* Premature rupture of membranes
* Chorioamnionitis
* Preoperative haemoglobin level below 10g/dl
* Body mass index (BMI) above 35kg/m2
* Any comorbidity (e.g. diabetes, hypertension, pre-eclampsia, eclampsia)
* Smoking and/or alcohol use
* The need for a blood transfusion.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06761495
Study Brief:
Protocol Section:
NCT06761495