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 @ 6:47 PM
Ignite Modification Date:
2025-12-24 @ 6:47 PM
NCT ID:
NCT05479357
Eligibility Criteria:
Inclusion Criteria:
* • High risk patients for post-partum hemorrhage who will subjected to Caeserean section either elective or in labour at or after 36 weeks of gestation. This should include one or more of the following:
1. History of postpartum hemorrhage.
2. Delivery of a macrosomic baby (\> 4000 g).
3. Multiple gestation.
4. Polyhydramnios.
5. Grand Multiparity.
6. Interstitial or submucous fibroid. (Single larger than 4 cm or Multiple myomata)
7. Chorioamnionitis.
Exclusion Criteria:
* • Patients without high risk for post-partum hemorrhage.
* Patients at high risk for postpartum hemorrhage but will deliver vaginally.
* Patients with medical disorders complicating pregnancy.
* Patients with coagulation defects.
* Preterm pregnancies.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT05479357
Study Brief:
Protocol Section:
NCT05479357