Could a common sugar fuel liver damage?
NCT ID NCT07013916
First seen Jul 31, 2026 · Last updated Jul 31, 2026
Summary
This trial asks whether fructose, a sugar found in fruit and processed foods, causes more liver inflammation in people with MASH (a serious fatty liver disease) than in those with milder fatty liver or no liver disease. Over four weeks, participants follow a low-sugar diet and then add either fructose or glucose supplements. Researchers compare blood, urine, and stool samples to see if fructose triggers inflammation and affects liver fat and gut bacteria.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- fructose (a type of sugar) compared with glucose (another type of sugar)
- What this could lead to
- If fructose is shown to trigger more inflammation in MASH, this could point toward dietary advice or treatments that limit fructose to slow liver damage.
- What could go wrong
- This is a small, short-term study, so results may not apply to everyone. It looks at markers of inflammation, not long-term outcomes like cirrhosis or liver cancer.
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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About 72 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Apr 2027
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.
- Ages
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45 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Able and willing to give written informed consent * Age 45-65 at consent * HbA1c \< 48 mmol/mol * Overweight and stage I obesity using BMI thresholds adjusted for ethnicity: * 23.0kg/m2 - 32.4kg/m2 in South Asian, Chinese, other Asian, Middle Eastern, Black African or African-Caribbean populations * 25kg/m2 - 34.9kg/m2 in White populations MASH Patients: Clinical diagnosis of MASH and F2 - F3 fibrosis: Either: Liver biopsy within 12 months of baseline Or: • History of histologically-diagnosed MASH with current evidence of fatty liver, AST\>20 and Fibroscan CAP≥248 dB/m and stiffness 9.5kPa -14kPa Or: • FAST score \>0.67 Patients with steatosis: • defined by Fibroscan CAP≥248dB/m and stiffness \<7.9kPa. Healthy controls: • defined by Fibroscan CAP\<248dB/m and stiffness \<7.9kPa. Exclusion Criteria: * Unwilling or unable to give consent * Age \<45 or \>65 * Any form of diabetes mellitus * Currently pregnant * Known fructose intolerance or food allergy * Diagnosis of cirrhosis or Fibroscan stiffness \>14kPa * Current Child-Pugh B/C or episode of decompensation in last year * Non-MASLD liver disease known to participant (including viral hepatitis, auto-immune hepatitis, primary sclerosing cholangitis, primary biliary cholangitis, haemochromatosis, sarcoidosis, cystic fibrosis, sickle cell disease) * Regular alcohol intake \> 14 units a week for females and \>21 units a week for males (participant-reported) * Smoking, vaping or use of nicotine-containing products within the last month * Taking prohibited medication: * Probiotic or antibiotic use within last 4 weeks (Note: participants will be considered eligible if they have undergone a 4-week washout from probiotics or 4-weeks after discontinuing antibiotic use) * any oral steroids within the last 6 weeks * current, or within 3 months, use of immunosuppressive medication * Amiodarone, nitrofurantoin, or anti-fungals within 3 months * Use of anti-obesity medication - orlistat or GLP-1 receptor agonist-containing treatments within 6 months * Use of vitamin E, pioglitazone or other medication for MASH including current or within 3 months enrolment in clinical trial unless documented to have been on placebo * History of malignancy (except basal cell carcinoma), or medication for malignancy within the last 2 years * Any major organ transplant (excluding corneal or hair) * Clinical diagnosis of chronic kidney disease 3 or above, or of heart failure (NYHA 3 or 4) * COPD requiring home oxygen * Known eating disorder (e.g. anorexia nervosa) or severe mental illness (e.g. schizophrenia) * Investigator opinion that study is unsuitable for patient
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Blizard Institute, Faculty of Medicine and Dentistry, Queen Mary University of London
RECRUITINGLondon, E1 2AT, United Kingdom
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Royal London Hospital
RECRUITINGLondon, E1 1FR, United Kingdom
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