Zapping the brain to heal the liver: new trial tests TMS for fatty liver
NCT ID NCT07399600
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a non-invasive brain stimulation technique called rTMS can reduce liver fat in people with alcohol-related fatty liver disease (MetALD). 105 participants will receive either personalized rTMS, standard rTMS, or a sham (placebo) treatment over 20 sessions. The goal is to see if targeting a deep brain reward center can improve liver health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- repetitive transcranial magnetic stimulation (rTMS)
- What this could lead to
- If it works, this could offer a non-invasive, drug-free way to reduce liver fat and improve metabolic health in people with alcohol-related fatty liver disease.
- What could go wrong
- This is an early-stage trial with only 105 participants, so results may not apply to everyone. The treatment is experimental, and its long-term benefits or risks are not yet known.
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
-
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
-
About 105 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Feb 2026
An estimate. Start dates often move.
- Expected to finish
-
Dec 2027
An estimate. End dates often move.
- Lead sponsor
-
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
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * Participants are able to understand the study protocol, requirements, and restrictions, are fully informed of potential adverse events, are willing to comply with follow-up visits, and voluntarily sign the informed consent form before enrollment. * Meet the diagnostic criteria for MASLD according to the Guidelines for the Prevention and Treatment of Metabolic (Non-Alcoholic) Fatty Liver Disease (2024 Edition), and fulfill the European definition of MetALD with moderate alcohol consumption (20-50 g/day for women; 30-60 g/day for men). * Age between 18 and 65 years. * Body mass index (BMI) \> 24 kg/m². * No history of alcohol abuse. Exclusion Criteria: * Contraindications to magnetic resonance imaging (MRI) or transcranial magnetic stimulation (TMS). * Mild cognitive impairment, defined as Montreal Cognitive Assessment (MoCA) score \< 25. * Severe comorbid somatic diseases or neurological disorders. * History of psychiatric disorders, or current use of antipsychotic medications. * Pregnant or breastfeeding women, or those planning pregnancy. * Previous TMS treatment within the last 3 months.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Fatty liver are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
The Affiliated Hospital of Hangzhou Normal University
Hangzhou, Zhejiang, 310015, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a weekly weight drug quiet gout attacks?
- Can a Once-Daily form of tacrolimus spare liver transplant patients from side effects?
- Ketogenic diet vs mediterranean diet: which better reshapes metabolism?
- Can tailoring bypass length improve weight loss surgery results?
- Can AI predict your lifespan from a short video?
- Do obese children with autism face different heart risks?