Placenta-Cervical Interface Angle for Predicting Placenta Accreta Spectrum Severity
Condition(s) studied
Investigational drug(s) / intervention(s)
Pregnant women at risk of PAS: Transvaginal ultrasonography performed in the sagittal plane to measure the Placenta-Cervical Interface Angle (PCIA), defined as the angle between the longitudinal axis of the cervical canal and the tangent to the lower placental edge, together with assessment of classic sonographic PAS markers.
Study summary
Placenta accreta spectrum (PAS) is associated with substantial maternal and neonatal morbidity, and accurate antenatal prediction of its severity remains challenging. Although several sonographic markers exist, most are subjective and operator-dependent, and few predict surgical complexity or adverse perinatal outcomes. This prospective observational cohort study evaluates the Placenta-Cervical Interface Angle (PCIA), a novel geometric transvaginal ultrasound marker, defined as the angle between the longitudinal axis of the cervical canal and the tangent line drawn to the lower placental edge. The study assesses the predictive performance of the PCIA for severe PAS and its association with intraoperative morbidity and adverse perinatal outcomes.
Eligibility
Primary outcome measure(s)
- Predictive performance of the Placenta-Cervical Interface Angle (PCIA) for severe placenta accreta spectrum — From antenatal ultrasound (>=20 weeks) to postoperative histopathological confirmation at delivery
Diagnostic accuracy of the sonographically measured PCIA for predicting surgically or histologically confirmed severe PAS, expressed as area under the ROC curve (AUC), sensitivity, specificity, and positive and negative predictive values. The optimal cut-off is determined by the Youden index.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Necmettin Erbakan University, Faculty of Medicine, Perinatology Clinic | Konya | Konya |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07832019 on ClinicalTrials.gov ↗ ← All trials in Turkey