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:
2026-03-26 @ 3:14 PM
Ignite Modification Date:
2026-03-26 @ 3:14 PM
NCT ID:
NCT07337759
Eligibility Criteria:
Inclusion Criteria: Pregnant women who delivered at the Clinic of Gynecology and Obstetrics, University Clinical Centre of Serbia
* Singleton pregnancy
* Available placental examination after delivery
* Available clinical and perinatal outcome data
* Gestational age at delivery ≥24 weeks
Exclusion Criteria:
Multiple pregnancy (e.g., twins or higher-order gestations)
* Major congenital or chromosomal fetal anomalies
* Intrauterine fetal demise
* Conditions directly affecting placental weight (e.g., placental mosaicism)
* Incomplete clinical, placental, or histopathological data
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT07337759
Study Brief:
Protocol Section:
NCT07337759