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 @ 2:24 AM
Ignite Modification Date:
2025-12-25 @ 2:24 AM
NCT ID:
NCT03442634
Eligibility Criteria:
Inclusion Criteria:
* Term Singleton Pregnancy.
* Uncomplicated Elective Cesarean Section.
* Time of Cesarean Section doesn't exceed 90 minutes.
* Average blood loss during and after cesarean section (doesn't exceed 1000cc).
* All patients will be under spinal anesthesia.
Exclusion Criteria:
* Postpartum Hemorrhage.
* Surgical Complications Such as intestinal injury.
* Medical disorders such as Diabetes and Hypertension
* Factors that may influence postpartum blood loss as anemia, multiple pregnancy and polyhydraminos.
* Use of tocolytic drugs
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT03442634
Study Brief:
Protocol Section:
NCT03442634