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 @ 9:42 PM
Ignite Modification Date:
2025-12-24 @ 9:42 PM
NCT ID:
NCT03266432
Eligibility Criteria:
Inclusion Criteria:
* ASA physical status I or II
* Age: ≥ 18 years
* Patients with all types of placenta previa
* Eligible for general anesthesia
* Elective cesarean section
* Singleton term pregnancy
* Normal coagulation profile: prothrombin time (PT), activated partial thromboplastin time (aPTT), the platelet count, fibrinogen level
Exclusion Criteria:
* Parturient refusal
* Known coagulopathy
* Women with a history of cardiac, respiratory, renal, neurologic or endocrine diseases.
* Eclampsia and preeclampsia
* Emergency surgeries
* Foetal abnormalities
* Drug induced thrombocytopenia as antibiotics
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT03266432
Study Brief:
Protocol Section:
NCT03266432