Clinical Trials Directory

Trials / Completed

CompletedNCT07421180

Maternal Serum Adropin in Placenta Accreta Spectrum

Maternal Serum Adropin as a Potential Biomarker for Placenta Accreta Spectrum

Status
Completed
Phase
Study type
Observational
Enrollment
84 (actual)
Sponsor
Adana City Training and Research Hospital · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Aim: To compare maternal serum adropin levels in pregnancies complicated by placenta previa and/or placenta accreta spectrum (PAS) with those of healthy pregnant women and to evaluate the diagnostic value of adropin for predicting placental invasion. Methods: This cross-sectional study included 84 singleton pregnancies at ≥34 weeks of gestation: 42 women diagnosed with placenta previa and/or PAS and 42 healthy pregnant women who underwent cesarean delivery. Maternal serum adropin levels are measured preoperatively using enzyme-linked immunosorbent assay. Demographic, obstetric, ultrasonographic, and intraoperative findings were recorded. Receiver operating characteristic (ROC) curve analysis is performed to assess the predictive performance of adropin for PAS.

Conditions

Timeline

Start date
2024-05-15
Primary completion
2025-04-01
Completion
2025-04-01
First posted
2026-02-19
Last updated
2026-02-20

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07421180. Inclusion in this directory is not an endorsement.