Ireland
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Starting soon Observational

Placenta-Cervical Interface Angle for Predicting Placenta Accreta Spectrum Severity

NCT07832019 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-09-15
Last updated
2026-09-21

Condition(s) studied

Placenta Accreta SpectrumPlacenta PreviaPlacenta Accreta

Investigational drug(s) / intervention(s)

Pregnant women at risk of PAS

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

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Gestational age greater than 20 weeks * Placenta previa or low-lying placenta * Suspected placenta accreta spectrum * History of cesarean delivery Exclusion Criteria: * Major fetal anomaly * Multiple pregnancy * Uterine malformation * Inadequate image quality * Active vaginal bleeding

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)

FacilityCityRegionStatus
Necmettin Erbakan University, Faculty of Medicine, Perinatology Clinic Konya Konya
Official registry record

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