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Clinical Trials in Italy / NCT06876805
Recruiting Observational

The Role of Ceus in the Characterization of Focal Liver Lesions Indeterminate to Second-level Methods

NCT06876805 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Phase
Observational
Started
2024-08-01
Last updated
2025-03-14

Condition(s) studied

Focal Liver Lesion

Investigational drug(s) / intervention(s)

CEUS or Contrast enhanced Ultrasound

CEUS or Contrast enhanced Ultrasound: CEUS performed as normal clinical practice

Study summary

The primary objective of the study is to determine the accuracy of CEUS in characterizing (as benign or malignant) focal liver lesions for which CT, MRI and/or PET have not been conclusive.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years. * CEUS performed performed in the last 6 months a CT, MRI and/or PET not decisive in characterizing a liver lesion. * Obtaining informed consent. Exclusion Criteria: * Technical impossibility to perform the ultrasound evaluation. * Documented allergy to the ultrasound contrast medium.

Primary outcome measure(s)

  • CEUS diagnostic accuracy — 2 years
    CEUS diagnostic accuracy in determining the nature of focal liver lesions

Trial sites (1)

FacilityCityRegionStatus
Policlinico Sant'Orsola Malpighi Bologna Italy Recruiting

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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 NCT06876805 on ClinicalTrials.gov ↗ ← All trials in Italy