Blood tests may spot hidden liver damage in diabetics
NCT ID NCT04232293
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at whether two blood tests, eLIFT and FibroMeter, can accurately detect liver fibrosis (scarring) in people with type 2 diabetes. The researchers compared these blood tests to standard methods like FibroScan and liver biopsy. The goal is to find a simpler, less invasive way to screen for liver damage in this high-risk group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If these blood tests prove accurate, they could offer a simple, non-invasive way to screen for liver fibrosis in people with type 2 diabetes, reducing the need for liver biopsies.
- What could go wrong
- This is a completed diagnostic study, not a treatment trial. The blood tests may not be accurate enough to replace current methods, and results may not apply to all patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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722 people
The number who actually took part.
- Started
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Jun 2021
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 40 years old, * Type 2 diabetes mellitus for more than 6 months, * BMI \> 25 kg/m2, * Waist circumference \> 94 cm (male) or 80 cm (female). * Patient benefiting from a social security system. Exclusion Criteria: * Medical follow up for liver disease, * Decompensated cirrhosis, * Health status that does not allow the participation of the patient, * Hospitalisation for acute complication: sepsis, infection, foot's ulcer, acute coronary syndrome,… * HbA1c \> 11,0 %, * Pregnancy. * Patient under guardianship or curatorship or protection of justice * Involvement refusal.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU d'Angers
Angers, 49100, France
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CHU de Nantes
Nantes, 44093, France
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