Skip to content

Evaluation of Liver Damage in Patients With Anorexia Nervosa by Blood Biomarker Analysis

BILAN: Evaluation of Liver Damage in Patients With Anorexia Nervosa by Blood BIomarker ANaLysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06262165
Acronym
BILAN
Enrollment
19
Registered
2024-02-15
Start date
2024-02-16
Completion date
2025-06-27
Last updated
2026-04-17

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

Conditions

Anorexia Nervosa

Keywords

Biomarkers, Liver fibrosis, Liver steatosis, Anorexia nervosa, Enteral refeeding

Brief summary

The main goal of the BIocoLlection in Anorexia Nervosa-liver damage evaluation BILAN study the blood biomarkers associated with liver cytolysis.

Detailed description

Study of the association between blood biomarkers and the presence of hepatic cytolysis, defined by AST and/or ALT above normal.

Interventions

OTHERPatients with Anorexia Nervosa

Patients with Anorexia Nervosa hospitalized for malnutrition

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

: * Patient over 15 years old * Diagnosis of Restricted Eating Disorders including Anorexia Nervosa according to the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) * Admission to Nantes University Hospital.

Exclusion criteria

: * Chronic active viral hepatitis * Hemochromatosis * Other genetic, autoimmune. * Treatment with a drug known to induce fatty liver disease (amiodarone, carbamazepine, tamoxifen, valproate, clozapine, anti-retrovirals) unless the dose has been stable for ≥ 3 months * Excessive alcohol consumption (≥ 30 grams per day in men, ≥ 20 grams per day in women) * Pregnant, parturient or breast-feeding women, persons deprived of liberty, adults under legal protection or unable to express their consent, persons not affiliated or not beneficiaries of a social security scheme, persons under guardianship or curators

Design outcomes

Primary

MeasureTime frameDescription
Identification of new blood biomarkers and hepatic cytolysisTwo yearsIdentify changes in concentration of new blood biomarkers in patients suffering from hepatic cytolysis, defined by aspartate transaminases (AST) and/or alanine transaminases (ALT) above normal values, compared to those with normal enzyme levels.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026