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 @ 2:25 PM
Ignite Modification Date:
2025-12-24 @ 2:25 PM
NCT ID:
NCT05664659
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women planning to deliver by CS.
* Age between 18-40.
* Gestational age: (36-42 weeks).
Exclusion Criteria:
1. Women in active labour.
2. Rupture of membranes more than 24 hours \&/or intraamniotic infection.
3. Suspected extensive adhesions eg: more than P3CS, endometriosis, previous pelvic surgery.
4. Antepartum hemorrhage and abnormal placentation e.g.: low lying placenta, placenta previa, placenta accreta.
5. Major intrapartum hemorrhage more than 1000 ml.
6. History of postpartum hemorrhage.
7. Anemia (Hb level less than 10g/dl).
8. Uterine overdistention eg: polyhydramnios, macrosomic baby, multiple pregnancy.
9. Known allergy to any of misoprostol, oxytocin, carbetocin.
10. Known medical disorders: Diabetes Mellitus, hypertensive disorders, Systemic Lupus Erythematosus.
11. Known coagulopathy problem.
12. Contraindication \&/or refusal to spinal anesthesia.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT05664659
Study Brief:
Protocol Section:
NCT05664659