Development of a Non-invasive Screening Tool to Predict Metabolic Dysfunction-associated Steatotic Liver Disease
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Bioimpedence Vector Analysis.
- Who it may be relevant to
- Registry conditions: Healthy, Fatty Liver, MASLD, MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Development of a Non-invasive Screening Tool to Predict Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) in Volunteers on Clinical Trials Utilising Machine-learning and Bioimpedance Vector Analysis
Overview
A generic screening study to establish structural and/or functional baselines of specific organs.
Detailed description
Fatty liver disease is a common condition (25% of the population) which can lead to liver inflammation, liver scarring and even liver cancer. Clinical trials are often performed in healthy volunteers, who may have underlying fatty liver without knowledge of it. In clinical trials fatty liver can both mean volunteers have abnormal liver tests, preventing them joining the trial, as well as more likely to have a possible liver drug reaction, causing volunteers to withdraw from a clinical trial of a new drug.
The principal objective of the study is to develop a clinical scoring tool that can accurately predict fatty liver disease in study volunteers, without the need for invasive tests (such as a tissue biopsy).
We aim to recruit initially 2000 volunteers to this study, both healthy volunteers and patients with known MASLD.
Volunteers will attend the unit to undergo all assessments on one day. Once consent is given with a study research physician, bloods will be taken and body measurements made (including BMI, weight, waist circumference). A full medical history and physical examination will then be performed by the research physician.
Bioimpedance body composition analysis will then be performed on an ACUNIQ device. Finally ultrasound of the liver and fibroscan will be performed. Once all assessments are complete the study volunteer will be discharged from the unit.
Once all results are finalised, analysis will be performed on all the data to create a clinical score to predict the presence of MASLD, both with statistical and machine learning methods.
Interventions
- Diagnostic test Bioimpedence Vector Analysis
Bioimpedence vector analysis
Primary outcome measures
- Establishment of Classification Tool for Use in Clinical Trials [Time frame: Study duration (1 year)]
Secondary outcome measures (1)
- Normal LFT Range in NAFLD patients [Time frame: Study duration (1 year)]
Eligibility criteria
Inclusion criteria
- Male or female volunteers aged ≥18 to ≤80 years at the date of signing the informed consent.
- Willingness and ability to provide written, personally signed, and dated informed consent, in accordance with the latest ICH Good Clinical Practice (GCP) Guidelines and applicable regulations.
- An understanding, ability and willingness to fully comply with project procedures and restrictions.
For PART B only:
1\. With a known history of MASLD as evidenced either of:
- GP diagnosis on HCF
- Documented Fibroscan or liver US demonstrating MASLD
Exclusion criteria
- Known alcoholic liver disease, history of cirrhosis of any other cause (metabolic, viral hepatitis or other)
- Any other significant previous liver pathology (liver malignancy, portal hypertension, infiltrative liver disease)
- Alcohol consumption >30 units per week
- An Implanted cardiac devices
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
United Kingdom · 1 center
- Richmond Pharmacology Ltd. 1a Newcomen St, London Bridge — London
Identifiers
NCT: NCT04873258 · C19030