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Recruiting Observational

Diagnosis and Outcomes of Placental Accretism

NCT06833606 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2023-07-17
Last updated
2025-02-19

Condition(s) studied

Placenta Accreta

Study summary

The goal of this observational study is to evaluate the diagnostic ability of the main criteria currently adopted for the diagnosis of placenta accreta and to define the maternal outcomes in terms of complications of the different management strategies currently adoptable when placental accretism is suspected.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
44 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 18 years and 44 years * Pregnant women with suspected placental accretism * Acquisition of informed consent form Exclusion Criteria: None

Primary outcome measure(s)

  • Frequency of correspondence between prenatal diagnosis and intra-operative finding of placental accretism — Up to 1 month post-partum
    disappearance of the hypoecogenaretroplacental stria, lacunae placental vasculature, hypervascularization of the utero-vesical interface, interruption/irregularity of the bladder will be assessed by ultrasound

Trial sites (7)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Bologna Recruiting
Ospedale "M. Bufalini" Cesena Forlì-Cesena Recruiting
Ospedale "Morgagni-Pierantoni" Forlì Forlì-Cesena Recruiting
AOU Policlinico di Modena Modena Modena Recruiting
Azienda Ospedaliero - Universitaria di Parma Parma Parma Recruiting
Arcispedale Santa Maria Nuova Reggio Emilia Reggio Emilia Recruiting
Ospedale "Infermi" di Rimini Rimini Rimini Recruiting
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 NCT06833606 on ClinicalTrials.gov ↗ ← All trials in Italy