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

NCT01306110 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 277

Last updated 2016-01-08

No results posted yet for this study

Summary

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

Conditions

Sponsors & Collaborators

  • Association HGE CHU Bordeaux Sud

    lead OTHER

Principal Investigators

  • Victor De Ledinghen, MD PhD · University Hospital, Bordeaux

  • Juliette Foucher, MD · University Hospital, Bordeaux

  • Julien Vergniol, MD · University Hospital, Bordeaux

  • Vincent Rigalleau, MD PhD · University Hospital, Bordeaux

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01306110 on ClinicalTrials.gov