← Back to Clinical Trials
RecruitingNCT06876805

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

◆ AI Clinical Summary
Plain-language summary for patients

Trial Parameters

ConditionFocal Liver Lesion
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
Study TypeOBSERVATIONAL
PhaseN/A
Enrollment100
SexALL
Min Age18 Years
Max AgeN/A
Start Date2024-08-01
Completion2026-08-01
Interventions
CEUS or Contrast enhanced Ultrasound

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief 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 Criteria

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.

Related Trials