ClinicalTrials.Veeva

Menu

Screening for Liver Fibrosis by Using Non-invasive Methods in Patients With Diabetes. A Prospective Study (DIABSCAN)

A

Association HGE CHU Bordeaux Sud

Status

Completed

Conditions

Diabetes

Study type

Observational

Funder types

Other

Identifiers

NCT01306110
FS02-062007

Details and patient eligibility

About

The aim of this study is to evaluate liver fibrosis using FibroScan and biochemical markers in patients with diabetes.

Full description

Patients with diabetes are at risk for nonalcoholic fatty liver disease (NAFLD) leading to advanced fibrosis, cirrhosis, and liver cancer. However, liver fibrosis screening in this large population needs non-invasive methods. Recently, FibroScan was shown to be a good method for the diagnosis of advanced fibrosis in NAFLD patients. We examined the efficacy of a screening strategy with a noninvasive fibrosis biomarker (FibroTest) and transient elastography (FibroScan) in patients with diabetes.

Enrollment

277 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female subjects
  • More than 18 years of age
  • Patients with Diabetes
  • Written informed consent

Exclusion criteria

  • Patients refusing to participate to the study and to provide written informed consent

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems