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PreDEA Study, Prevention in Emergency / Acceptance Departments: the Case of Hepatic Steatosis

U

University of L'Aquila

Status

Enrolling

Conditions

Hepatic Steatosis

Treatments

Device: liver ultrasound

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Our study aims to evaluate whether the Emergency Department (PS) can support the health system to improve the prevention and management of chronic inflammatory diseases and ensure actions aimed at screening, raising awareness and informing the population.

Specifically, the determination of the prevalence of a widely diffused pathology such as fatty liver disease aims to be the precursor of future pilot studies aimed at evaluating the advantages and critical issues of the PS as a prevention tool.

Enrollment

20,189 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients over 18
  • Patients admitted to Emergency department in white or green code

Exclusion criteria

  • Patients under 18
  • Patients admitted to Emergency department in yellow or red code

Trial design

20,189 participants in 2 patient groups

presence of hepatic hyperechogenicity on ultrasound evaluation
Treatment:
Device: liver ultrasound
absence of hepatic hyperechogenicity on ultrasound evaluation
Treatment:
Device: liver ultrasound

Trial contacts and locations

1

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Central trial contact

Clara Balsano, MD

Data sourced from clinicaltrials.gov

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