Scientists hunt for clues in body fluids to predict liver failure outcomes
NCT ID NCT02833064
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study aims to find biological markers in blood, urine, stool, and breath that can predict how patients with acute liver injury or failure will fare. Researchers will collect samples daily for up to seven days from 200 participants, and a small group will also undergo MRI scans. The goal is to better understand the disease and improve care.
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 successful, this could help doctors predict complications and outcomes in liver failure, guiding better treatment decisions.
- What could go wrong
- This is an observational study, not a treatment trial. It may not identify clear biomarkers, and findings may not apply to all patients.
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.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2016
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- 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.
Who is studied
1. Acute liver failure 2. Acute liver injury 3. Acute on chronic hepatic failure 4. Stable cirrhotics 5. Non-cirrhotic liver disease
- Ages
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16 to 80 years
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * acute liver injury (newly deranged liver function tests (LFTs) and coagulopathy with International Normalized Ratio (INR) \>1.5 in absence of chronic liver disease) * acute liver failure ( as above, plus hepatic encephalopathy) * acute on chronic liver failure (worsening of LFTS and development of at least 1 organ failure in patient with cirrhosis) * stable cirrhosis * non-cirrhotic liver disease Exclusion Criteria: * refusal of consent * withdrawal of consent
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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.
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Other studies related to the condition(s) this trial covers.
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