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Screening of NASH in Oupatients Followed in Various Hospital Specialty Clinics at the University Hospital of Strasbourg

Screening of NASH in Oupatients Followed in Various Hospital Specialty Clinics at the University Hospital of Strasbourg

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04282447
Acronym
NASH-SPE
Enrollment
600
Registered
2020-02-24
Start date
2020-08-14
Completion date
2022-05-31
Last updated
2020-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nonalcoholic Fatty Liver Disease

Brief summary

The aim of the present study is to assess, by using a simple algorithm combining FIB-4 and Fibroscan, the prevalence of NASH with advanced fibrosis in outpatients followed in various hospital specialty clinics other than hepato/gastroenterology and to examine risk factors associated with this condition. The prevalence of NASH will be investigated among 6 cohorts of outpatients followed in different hospital specialty clinics at Hôpitaux Universitaires de Strasbourg.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age ≥ 18 years * outpatients followed at specialty clinics in HUS and at risk of NAFLD: with at least one metabolic risk factor (overweight, diabetes mellitus, hypertension, hypertriglyceridemia) and/or elevated transaminases and/or liver steatosis on US. * endocrinology cohort : type 2 diabetes patients * infectious disease cohort : HIV positive patients * rheumatology cohort : patients with psoriasis, gout or rheumatoid arthritis * nephrology cohort : patients with chronic kidney disease such as diabetic nephropathy or hypertensive nephropathy, including those receiving hemodialysis. * cardiology cohorts: patients with history of angina, myocardial infarction, stroke or arteritis of lower limbs. * internal medicine cohort: patients with auto immune systemic diseases such as lupus, sclerosis or rheumatoid arthritis. * subjects who have given their informed consent * Subjects affiliated to a social security system

Exclusion criteria

* alcohol consumption \> 30g/d in male or \> 20g/d in female in the past 6 months * history of chronic viral hepatitis * history of liver auto immune disease, genetic hemochromatosis, Wilson disease * biliary disease, bile duct obstruction * drug-induced liver injury * secondary liver cancer or other active cancer * organ graft * use of medications associated with secondary NAFLD (corticosteroids, tamoxifen, amiodarone, methotrexate). * congestive heart failure * AIDS * pregnancy, breastfeeding * no information could be given to the patient (subject faces emergency situation, comprehension difficulties, etc.) * patient under guardianship * patients under judicial protection

Design outcomes

Primary

MeasureTime frameDescription
Estimated prevalence of NASH with advanced fibrosis among several hospital specialty clinics3 monthsTo assess the estimated prevalence of NASH , calcul of the FIB4

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026