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NCT Number: NCT06907563

Long-term Follow-up to Determine Outcome in Liver Disease (LOVE Study)

The rational to conduct the LOVE study builds on the lack of available data on outcomes in steatotic liver disease in well characterized patients over a time frame of several years. At current limited data on liver-specific and overall outcome in patients with MASLD, MetALD and ALD are available. Liver histology is the only accepted surrogate to reasonably likely predict outcomes in patients with non-cirrhotic liver disease and is currently used in regulatory trials. To overcome the limitations of liver biopsy and use validated non-invasive tests (NITs) to predict outcomes, the LOVE study will be conducted based on existing cohort studies in well pheno- and genotyped patients and will inform on the relevant outcomes based on baseline and ongoing biomarker assessment. The overarching goal is to qualify a NIT for patient identification and preventive measures in the regulatory context.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Previous Informed consent for cohort studies
  • > 18 years of age
  • Diagnosis of SLD (MASLD, MetALD, ALD)

Exclusion criteria

  • No consent for previous cohort studies
  • < 18 years of age
  • No Diagnosis of SLD (MASLD, MetALD, ALD)

Treatment and study plan

Primary outcomes

  1. Major-adverse liver outcomes (MALO)

    Time frame: 5 years follow-up time

    Development of cirrhosis. Hepatic decompensation: ascites, hepatic encephalopathy, spontaneous bacterial peritonitis, portal hypertension, varices.

  2. All-cause mortality

    Time frame: 5 years follow-up time

    Death during the follow-up period due to any cause

Secondary outcomes

  1. Health-related quality of life (HRQL)

    Time frame: 5 years

    To measure the impact on the health-related quality of life in patients during the natural history of the disease.

  2. Assess prognostic biomarkers and develop a novel tool to integrate them into a digital tool to predict outcomes

    Time frame: 5 years

  3. Major adverse cardiac events (MACE)

    Time frame: 5 years

  4. Development of relevant clinical outcomes

    Time frame: 5 years

    Incidence of cancer, chronic kidney disease, neurodegenerative disease, dementia, and depression

Study contacts

Contact information is provided by the study sponsor or research team.

Jörn M. Schattenberg, MD

CONTACT

[email protected]

+49684116 ext. 15027

Sponsors and collaborators

Lead sponsor

Universität des Saarlandes

Other

Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Barcelona Institute for Global Health
  • Hospital Clinic of Barcelona
  • Newcastle University
  • Odense University Hospital
  • Universitatsmedizin Mainz - 1. Medizinische Klinik
  • University of Turin, Italy

Registry information

Acronym: LOVE

Important dates

Study start
2025
Primary completion
2030
Study completion
2035
First posted
Apr 2, 2025
Registry last updated
Apr 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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