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Liver Status in Psychiatric Inpatients

Liver Status in Psychiatric Inpatients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05213442
Acronym
LIVERSPIN
Enrollment
450
Registered
2022-01-28
Start date
2022-04-06
Completion date
2023-12-15
Last updated
2024-02-14

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

Conditions

Psychiatric Illness

Brief summary

Adults hospitalized in psychiatry have an increased frequency of somatic disorders, in particular various liver diseases (viral hepatitis, non-alcohol related liver steatosis, alcohol related liver disease). The evaluation of these liver disorders in psychiatric inpatients remains very little explored in France, contributing to the poor overall medical status of psychiatric patients. The LIVERSPIN study aims to estimate the prevalence rates of liver pathologies in psychiatric inpatients and to explore the factors associated with the existence of a liver pathology

Detailed description

The LIVERSPIN study aims to estimate the prevalence rates of liver disease in psychiatric inpatients and to explore factors associated with the existence of liver disease. All hospitalized patients can potentially be recruited. They will benefit from the usual clinical and paraclinical examinations as part of their hospitalization diagnostic work-up. For the determination of biological analyses, a blood sample will be taken following inclusion as well as a Fibroscan examination.

Interventions

DIAGNOSTIC_TESTTo estimate the prevalence rates of liver disease in psychiatric inpatients and to explore factors associated with the existence of liver disease.

Patients will receive the usual clinical and paraclinical examinations as part of their hospitalization diagnostic workup. For the biological analyses, a blood sample will be taken following inclusion as well as a Fibroscan examination. Data will be collected from the patient, or if necessary from the health care team, using the medical record (interview and/or self-questionnaires).

Sponsors

Hospices Civils de Lyon
CollaboratorOTHER
Hôpital le Vinatier
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Monocentric, non randomized, non comparative cross-sectional study

Eligibility

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

Inclusion criteria

* Age \>18 years old * Social insurance * Current hospitalization in any psychiatric unit of the participating center * Adult or legal representative who has given written and informed consent to participate in the study. By default, the oral consent of the adult will be obtained (as well as the written consent of the legal representative) * Information given to the curator(for people under curatorship)

Exclusion criteria

* \- Clinical state of the patient which do not allow the collection of study data (according to the investigator)

Design outcomes

Primary

MeasureTime frameDescription
HCV diagnosisAt inclusionHCV diagnosis defined by positive HCV antibodies in blood

Secondary

MeasureTime frameDescription
HBV diagnosisAt inclusionHBV diagnosis defined by positive HBsAg in blood
HIV diagnosisAt inclusionHIV diagnosis defined by positive anti-HIV1 or anti-HIV2 antibodies in blood
Suspicion of NAFLDAt inclusionSuspicion of NAFLD on FIB-4 and the interrogation
Suspicion of alcoholic liver diseaseAt inclusionSuspicion of alcoholic liver disease on FIB-4 and the interrogation

Countries

France

Outcome results

None listed

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