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UDFF Performance Evaluation ((Ultrason Derived Fat Fraction)

U

University Hospital, Angers

Status

Enrolling

Conditions

Non Alcoholic Fatty Liver Disease

Treatments

Diagnostic Test: UDFF

Study type

Observational

Funder types

Other

Identifiers

NCT06080386
202300122

Details and patient eligibility

About

The purpose of this study is to assess UDFF performance (compared to MRI)

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients who had hepatic ultrasound with available UDFF measurements and hepatic MRI (with steatosis quantification sequences) between 01/01/2022 and 31/09/2023 may be included.

Exclusion criteria

  • chronic liver disease with a different etiology other than NAFL/NASH or mixed (hepatitis B or C, hemochromatosis, autoimmune hepatitis, Wilson's disease, cholestasic disease, alpha 1 antitrypsin deficiency),
  • decompensated cirrhosis (ascites, jaundice, encephalopathy, rupture of esophageal varices),
  • hepatocellular carcinoma.
  • opposition to the use of its data

Trial design

100 participants in 1 patient group

one group
Description:
Patients who had during their care UDFF ultrasound measurements and liver MRI over the study period may be included in this study
Treatment:
Diagnostic Test: UDFF

Trial contacts and locations

1

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Central trial contact

Christophe Aubé; Marie Bost

Data sourced from clinicaltrials.gov

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