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NCT Number: NCT06813508

Prognostic Factors for HCC and Liver Transplantation in Patients With MASLD/MASH

The BOMASH study is a single-center, prospective/retrospective observational study without pharmacological interventions. It will include all patients diagnosed with Metabolic-Associated Steatotic Liver Disease (MASLD/MASH), whether newly diagnosed or previously identified at the center during follow-up or as part of routine diagnostic and therapeutic care.

The aim of the study is to identify predictive factors related to the prognosis of patients with metabolic liver disease (MASLD/MASH). Specifically, the study seeks to uncover biomarkers that can identify individuals at risk of requiring a liver transplant or developing HCC.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, 40138, Italy

Location status: Recruiting

Location contact

Bernardo Stefanini, MD, PhD

SUB_INVESTIGATOR

Fabio Piscaglia, Prof, MD

CONTACT

[email protected]

+39 051 2142542

Fabio Piscaglia, Prof., MD

PRINCIPAL_INVESTIGATOR

Federico Ravaioli, MD, PhD

SUB_INVESTIGATOR

Mariarosaria Marseglia, Dr.

CONTACT

[email protected]

+39 0512142477

Silvia Ferri, MD, PhD

SUB_INVESTIGATOR

About this study

The BOMASH study is a single-center, prospective/retrospective observational study without pharmacological interventions. It will include all patients diagnosed with Metabolic-Associated Steatotic Liver Disease and Metabolic-Associated Steatohepatitis (MASLD/MASH), whether newly diagnosed or previously identified at the center during follow-ups or as part of routine diagnostic and therapeutic care. MASLD is characterized by significant variability in terms of severity and progression rates. Although a large portion of the population is at risk, only a minority develop liver-related comorbidities. Epidemiological studies reveal that patients with MASH have a higher risk of developing liver-related complications compared to those with simple steatosis (MASLD). However, the factors driving progression to MASH and its advanced stages remain unclear, and disease staging can only be accurately determined through liver biopsy. Given the large number of individuals at risk for MASLD, liver biopsy is not a feasible screening tool for widespread use. Key challenges involve understanding the biological and environmental factors that drive variability among MASLD patients and using this knowledge to develop effective methods for risk stratification, enabling targeted treatment for individuals at the highest risk.

The identification of risk factors through the combination of non-invasive tests (serum biomarkers and non-invasive techniques) can enable risk stratification for hepatocellular carcinoma (HCC) development and identify individuals who may require liver transplantation.

A study on MASLD represents a valuable tool to enhance understanding of this nosological entity and to support basic, clinical, and epidemiological research. It also benefits individuals affected by these conditions and assists national and local authorities in planning and optimizing healthcare and social services. Systematic data collection on MASLD can be instrumental in identifying previously unrecognized risk factors that may predispose individuals to more aggressive and treatment-resistant forms of the disease.

Analyzing the collected data could highlight potential common markers among patients whose MASLD diagnosis progresses to HCC and subsequently necessitates liver transplantation. These findings would provide useful prognostic factors for patient management.

In conclusion, the opportunity to longitudinally track disease progression in a large cohort of patients with chronic metabolic liver disease could pave the way for strategies that make the management of this highly prevalent condition more sustainable for national and regional healthcare systems.

Therefore, the aim of the study is to identify predictive factors related to the prognosis of patients with metabolic liver disease (MASLD/MASH). Specifically, the study seeks to uncover biomarkers that can identify individuals at risk of requiring a liver transplant or developing HCC.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All patients with a diagnosis of MASLD, established according to the most recent published guidelines (EASL, EASD, EASO)
  • Age ≥18 years

Inclusion criteria

for Biological Sample Collection:

  • Patients requiring liver biopsy for diagnostic purposes, as indicated by the most recent published guidelines (EASL, EASD, EASO)

Exclusion criteria

  • No exclusion criteria.

Treatment and study plan

Primary outcomes

  1. Number of hepatocellular carcinoma (HCC) or liver transplantation (OLT) cases and time to onset.

    Time frame: From enrollment to november 2044

    The aim of the study is to identify predictive factors related to the prognosis of patients with liver disease of dysmetabolic origin: Metabolic-Associated Steatotic Liver Disease and Metabolic-Associated Steatohepatitis (MASLD/MASH). Specifically, the aim is to identify markers that can predict individuals who will later require a liver transplant or develop hepatocellular carcinoma.

Secondary outcomes

  1. Incidence of HCC and liver transplantation (OLT)

    Time frame: From enrollment to november 2044

    Calculate the incidence of liver transplantation and the occurrence of HCC for this disease.

  2. Response rate in patients

    Time frame: From enrollment to november 2044

    Objective response rate in patients with HCC or those requiring liver transplantation, measured using RECIST 1.1 criteria.

  3. Number of cases of liver complications

    Time frame: From enrollment to november 2044

    Cases of liver decompensation, major adverse cardiovascular events (MACE), extrahepatic tumors, and liver transplantation, along with their time of onset.

  4. Response to dietologic and pharmacological therapies related to glycated hemoglobin levels

    Time frame: From enrollment to november 2044

    Positive response to dietetic and drug therapies is measured by glycated hemoglobin levels.

  5. Response to dieto-therapeutic and pharmacological therapies related to weight

    Time frame: From enrollment to november 2044

    Positive response to dietetic and pharmacological therapies is measured by weight loss.

  6. Response to dieto-therapeutic and pharmacological therapies related to biochemical parameters

    Time frame: From enrollment to november 2044

    Positive response to dietetic and pharmacological therapies is measured by biochemical parameters (Aspartate amino transferase, Alanina amino transferase).

  7. Number of HCC or liver transplantation (OLT) cases categorized by MASLD and MASH

    Time frame: From enrollment to november 2044

Study contacts

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

Fabio Piscaglia, MD

CONTACT

[email protected]

+39 051 2142542

Federico Ravaioli, MD PhD

CONTACT

[email protected]

+39 0512142717

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Official study title

Prognostic Factors for the Development of Hepatocellular Carcinoma (HCC) and Indications for Liver Transplantation in Patients With Metabolic Liver Diseases (MASLD/MASH): The BOMASH Study

Acronym: BOMASH

Important dates

Study start
2024
Primary completion
2043
Study completion
2044
First posted
Feb 7, 2025
Registry last updated
Feb 7, 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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