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Clinical Trials in Spain / NCT06838468
Enrolling by invitation Observational

cACLD in Patients With Alcohol Use Disorder in the Hospital Detoxification Unit

NCT06838468 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2024-03-06
Last updated
2025-02-20

Condition(s) studied

Liver Disease ChronicCirrhosisDetoxificationAlcohol Abuse/Dependence

Investigational drug(s) / intervention(s)

Screening of compensated advance chronic liver disease

Screening of compensated advance chronic liver disease: The tests performed will include a general blood analysis to evaluate liver and kidney function, an assessment of the prevalence of metabolic diseases such as obesity, hypertension, or diabetes, an abdominal ultrasound, and elastography to assess liver stiffness. Another intervention to be studied is whether the request for diagnostic tests to evaluate liver disease, as well as the visit of the hepatologist during hospitalization in the detoxification unit, influences subsequent alcohol abstinence. To this end, abstinence will be assessed six months after admission to the alcohol detoxification unit and compared with a retrospective cohort of patients admitted to the detoxification unit one year ago, in whom no liver disease evaluation was conducted neither information of potencial liver damage was offered by hepatologist and the intervention was carried out only by the psychiatrists responsible for the unit.

Study summary

The aim of this study is to conduct a quick assessment of potential liver damage caused by chronic alcohol consumption. Taking advantage of the patient's admission to a specialized detoxification unit, several tests will be performed to determine the extent of liver damage through blood tests, ultrasound, and FibroScan

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Patients admitted to the detoxification unit for alcohol use disorder * Patients admitted to the psychiatry unit for dual pathology with harmful alcohol consumption (\> 30 g/day in men (3 standard drinks) and \> 20 g/day in women (2 standard drinks)) Exclusion Criteria: * Refusal to undergo additional tests (blood analysis, ultrasound, and FibroScan)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Consorci Corporació Sanitària Parc Taulí Sabadell Barcelona

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06838468 on ClinicalTrials.gov ↗ ← All trials in Spain