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Updated May 2026 · ClinicalTrials.gov

RECRUITINGPhase 4INTERVENTIONAL

Fibrosis Lessens After Metabolic Surgery

A Prospective Multicenter International Randomized Controlled Trial Comparing Surgical and Medical Therapies in the Treatment of Advanced Metabolic Dysfunction Associated Steatohepatitis

Fibrosis Lessens After Metabolic Surgery (NCT06374875) is a Phase 4 interventional studying Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) and Non-Alcoholic Fatty Liver Disease, sponsored by Ali Aminian. RECRUITING as of the most recent ClinicalTrials.gov update. Talk to your doctor before contacting the trial site.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease (NAFLD), a major global public health concern, is commonly associated with obesity, diabetes, and dyslipidemia. MASLD is currently the most common cause of chronic liver disease affecting about 80% of people with obesity, ranging from simple fat deposits in the liver to Metabolic Dysfunction-Associated Steatohepatitis (MASH), cellular injury, advanced fibrosis, cirrhosis, or hepatocellular carcinoma. Patients with MASH are also at risk for cardiovascular disease and mortality. There is no universally approved medication for MASH. Weight loss remains the cornerstone of MASH treatment. Patients meeting the inclusion and exclusion criteria and who give informed consent will be enrolled in the trial and undergo the baseline liver biopsy (if none available). Approximately 120 patients with MASH and liver fibrosis (F1-F4 in baseline liver biopsy) will be randomized in a 1:1 ratio to metabolic surgery or medical treatment (incretin-based therapies ± other medical therapies for MASH) and followed for 2 years at which time a repeat liver biopsy will be performed for the assessment of the primary end point.

What Stage of Research Is This?

Phase 4 studies happen after a treatment has been approved by the FDA. They monitor long-term safety, real-world effectiveness, and any rare side effects that only emerge in larger populations over longer periods. Phase 4 results sometimes lead to label changes, additional warnings, or — rarely — withdrawal of approval.

This trial is currently recruiting participants. The sponsor has registered the study with ClinicalTrials.gov as actively enrolling, which means new applicants who meet the eligibility criteria can be considered for screening. Trial status can change between updates — confirm current recruiting status with the study contact before traveling for a screening visit.

Target enrollment of 120 participants puts this in the typical range for a Phase 2-style efficacy study or a moderate Phase 3 trial in a focused Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) subpopulation. At this scale, the study has enough statistical power to detect a clear treatment effect but is not the largest cohort in the field.

Who May Be Eligible (Plain English)

Inclusion Criteria Entry into the study would require that the patient: 1. Is a candidate for general anesthesia 2. Is eligible for metabolic surgery (RYGB or SG) based on the ASMBS/IFSO 2022 guidelines 3. Has insurance coverage for metabolic surgery (the requirements may vary in each country) 4. Is ≥18 and ≤75 years old at the time of signing the willing to sign a consent form 5. Has a BMI ≥35 and ≤70 kg/m2 at the time of first study visit 6. FIB-4 ≥ 1.3 7. At least one of the following 5 criteria suggesting presence of advanced fibrosis: - LSM ≥ 12 kPa by VCTE using FibroScan® - LSM ≥ 12 kPa by SWE - LSM ≥ 1.7 m/s by ARFI - LSM ≥ 3.63 kPa MRE - ELF score ≥ 9.8 8. Patients with and without T2DM are eligible for the study. Patients with T2DM should have been on a stable dose of anti-diabetic medication (including insulin but not semaglutide or tirzepatide or liraglutide) for at least 3 months prior to entry, with glycated hemoglobin (HbA1c) ≤12%. 9. Self-reported stable weight in 6 months before the first study visit (no weight loss \>10% within 6 months prior to the first study visit) a. In patients with a historical noninvasive tests or liver biopsy, weight loss of no more than 10% is allowed from 6 months prior to the historical tests until the first study visit 10. Has the ability and willingness to participate in the study, provide willing to sign a consent form, and agree to any of the arms involved in the study 11. Can understand the options and comply with the requirements of each arm, including one liver biopsy performed during the screening period (if no adequate biopsy within 12 months before screening is available) and one liver biopsy after 2-years 12. Has a negative urine pregnancy test at the first and at the randomization visits for women of childbearing potential. 13. Women of childbearing age must agree to use reliable method of contraception for 2 years 8.2 Exclusion Criteria ...See full criteria on ClinicalTrials.gov Always talk to your doctor about whether this trial is right for you.

These are translations of the protocol\'s inclusion and exclusion criteria, simplified for patients and caregivers. The original clinical text appears below. Eligibility is ultimately confirmed by the trial site\'s screening process — this summary is a starting point for a conversation with your doctor, not a final determination.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria Entry into the study would require that the patient: 1. Is a candidate for general anesthesia 2. Is eligible for metabolic surgery (RYGB or SG) based on the ASMBS/IFSO 2022 guidelines 3. Has insurance coverage for metabolic surgery (the requirements may vary in each country) 4. Is ≥18 and ≤75 years old at the time of signing the informed consent 5. Has a BMI ≥35 and ≤70 kg/m2 at the time of first study visit 6. FIB-4 ≥ 1.3 7. At least one of the following 5 criteria suggesting presence of advanced fibrosis: * LSM ≥ 12 kPa by VCTE using FibroScan® * LSM ≥ 12 kPa by SWE * LSM ≥ 1.7 m/s by ARFI * LSM ≥ 3.63 kPa MRE * ELF score ≥ 9.8 8. Patients with and without T2DM are eligible for the study. Patients with T2DM should have been on a stable dose of anti-diabetic medication (including insulin but not semaglutide or tirzepatide or liraglutide) for at least 3 months prior to entry, with glycated hemoglobin (HbA1c) ≤12%. 9. Self-reported stable weight in 6 months before the first study visit (no weight loss \>10% within 6 months prior to the first study visit) a. In patients with a historical noninvasive tests or liver biopsy, weight loss of no more than 10% is allowed from 6 months prior to the historical tests until the first study visit 10. Has the ability and willingness to participate in the study, provide informed consent, and agree to any of the arms involved in the study 11. Can understand the options and comply with the requirements of each arm, including one liver biopsy performed during the screening period (if no adequate biopsy within 12 months before screening is available) and one liver biopsy after 2-years 12. Has a negative urine pregnancy test at the first and at the randomization visits for women of childbearing potential. 13. Women of childbearing age must agree to use reliable method of contraception for 2 years 8.2 Exclusion Criteria Patients who meet the following criteria will be excluded from the study: 1. Known history of other chronic liver diseases (drug induced, viral hepatitis, autoimmune, and genetic): * Hepatitis B as detected by presence of hepatitis B surface antigen (HBsAg) * Hepatitis C as detected by presence of hepatitis C virus (HCV) RNA (in case the screening test for hepatitis C is positive, the confirmative test is decisive) * Autoimmune liver disease as diagnosed by antibodies or compatible liver histology * Primary biliary cirrhosis as defined by the presence of at least 2 criteria (elevated alkaline phosphatase, presence of anti-mitochondrial antibody, and histologic evidence of nonsuppurative destructive cholangitis and destruction of interlobular bile ducts) * Primary sclerosing cholangitis * Wilson's disease as diagnosed by low ceruloplasmin or compatible liver histology * Alpha-1-antitrypsin deficiency as diagnosed by alpha1-antitrypsin level or liver histology * Hemochromatosis as diagnosed by HFE mutations (C282Y, H63D), ferritin and transferrin saturation levels, or presence of 3+ or 4+ stainable iron on liver biopsy * Drug-induced liver disease diagnosed by medical history * Known bile duct obstruction * Suspected or proven liver cancer 2. Weight change \>10% within 6 months prior to the first study visit or prior to the historical liver biopsy 3. Treatment with semaglutide, tirzepatide, or liraglutide (for obesity or for T2DM) \<90 days before the first study visit. • However, patients are allowed to participate if they have been on a low dose (or are on older generation GLP-1 agonists) and have lost less than 10% of their body weight since starting the medication. 4. Type 1 diabetes or autoimmune diabetes 5. Known cases of human immunodeficiency virus infection 6. Prior bariatric and metabolic surgery of any kind • Reversed procedures such as gastric band or intragastric balloon that have been removed at least 3 months prior to the first study visit are allowed. 7. Prior complex foregut surgery including any esophageal and gastric surgeries, anti-reflux procedures, biliary diversion, and complex trauma surgery 8. Any surgery requiring general anesthesia within 1 month prior to signing the consent 9. History of solid organ transplant 10. Severe pulmonary disease defined as FEV1 \< 50% of predicted value 11. Significant cardiac or atherosclerotic disease (planned to undergo cardiac, coronary, carotid, or peripheral artery revascularization procedures in the next 12 months) 12. Severe uncompensated cardiopulmonary disease leading to American Society of Anesthesiologists Class IV or V 13. Classified as New York Heart Association Class IV 14. Left ventricular ejection fraction \<25% at the time of screening 15. Myocardial infarction, unstable angina, stroke, heart surgery, coronary stent placement in the past 6 months 16. Chronic renal insufficiency with eGFR below 30 mL/min/1.73 m2, or being on dialysis 17. Presence of large hiatal hernia (\>7 cm) 18. Presence of Crohn's disease 19. Psychiatric disorders including (but not limited to) dementia, active psychosis, severe depression requiring 3 or more medications, history of suicide attempts, active alcohol, or substance abuse within the previous 12 months that in the opinion of the investigators could disqualify the patient from metabolic surgery 20. Pregnancy, the intention of becoming pregnant, or not using adequate contraceptive measures 21. Breastfeeding 22. Diagnosis of malignancy within the preceding 3 years (except squamous cell and basal cell cancer of the skin) 23. Anemia defined as hemoglobin less than 9 g/dL 24. On therapeutic dose of anticoagulants such as warfarin or direct oral anticoagulants (DOACs) 25. Known history of clotting disorders, including pulmonary embolus and deep vein thrombosis 26. Clinical judgment that life expectancy is less than 3 years 27. Use of investigational therapy within 3 months prior to signing the consent 28. History of pancreatic carcinoma 29. Acute pancreatitis \< 180 days before screening 30. History or presence of chronic pancreatitis 31. Presence of concerning thyroid nodule 32. Uncontrolled thyroid disease: thyroid stimulating hormone (TSH) \> 6.0 mIU/L or \< 0.1 mIU/L before the first study visit * Patients receiving treatment for hypothyroidism can be included if their thyroid hormone replacement dose has been stable for at least 3 months. * Patients whose TSH is outside the rang but they have normal levels of thyroid hormones can be included. 33. A personal or family history of medullary thyroid carcinoma (MTC) or in patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2) 34. Evidence or history of ascites or spontaneous bacterial peritonitis that require(d) treatment • Trace ascites identified only by an abdominal imaging without other evidence of clinically significant portal hypertension and esophageal varices is not an exclusion criterion. 35. Evidence or history of hepatic encephalopathy 36. Evidence or history of variceal bleeding 37. Evidence or history of portosplenic vein thrombosis 38. Current or history of significant alcohol consumption for a period of more than 3 consecutive months within 1 year prior to the first study visit. • Defined as more than 14 units/week for females (\>1 drink per day) and more than 21 units/week for males (\>2 drinks per day) on average, where one unit of alcohol is equivalent to a 12-oz beer, 4-ounce glass of wine, or 1-ounce shot of hard liquor. 39. Treatment with medications (for more than 14 consecutive days) with known effect on liver steatosis (e.g., treatment with systemic corticosteroids \[oral or intravenous\], methotrexate, tamoxifen, valproic acid, amiodarone, or tetracycline) in the 3 months prior to the first study visit (or historical liver biopsy). 40. ALT or AST or Alkaline phosphatase \>200 U/L 41. Recurrent major hypoglycemia or hypoglycemic unawareness 42. Inability to safely obtain a liver biopsy 43. Any condition or major illness that, in the investigator's judgment, places the subject at undue risk by participating in the study 44. Unable to understand the risks, benefits, and compliance requirements of study 45. Lack capacity to give informed consent 46. Plans to move outside the primary location of study (country) within the next 24 months 47. Known or suspected allergy to semaglutide, tirzepatide, liraglutide, excipients, or related products 48. Previous participation in this trial and got randomized to one of the study groups but did not proceed. 49. Hospitalization due to COVID-19 within 2 months prior to screening. 50. Platelet count \<80,000 51. International Normalized Ratio (INR) \>1.7 52. Child-Pugh score B or C 53. MELD score ≥15 54. Upper endoscopy showing gastroesophageal varices 55. Upper endoscopy showing more than mild portal hypertensive gastropathy 56. Liver vascular ultrasound (duplex ultrasonography) showing significant portal hypertension characterized by dilated portal vein (\>13 mm), biphasic or reverse flow in the portal vein, enlarged paraumbilical veins, splenorenal collaterals, or dilated left and short gastric veins. Note: Negative findings on upper endoscopy and liver duplex ultrasound (done within one year of the first study visit for both tests) are necessary to establish eligibility for the FLAMES. * Ruling out clinically significant portal hypertension is particularly important in patients with a liver stiffness ≥20 kPa or with a platelet count \<150,000 per μL or with a (historical) liver biopsy showing cirrhosis. * A subset of patients without having upper endoscopy and liver duplex ultrasound can be eligible for enrollment if their: * liver stiffness (by transient elastography using FibroScan®) is between 12 and 15 kPa and their platelet count is \>150,000 per μL, or * a (historical) liver biopsy showing absence of cirrhosis, or * a (historical) HVPG \< 5 mmHg 57. Cross-sectional abdominal imaging (if available historically) indicating presence of large portosystemic collaterals or ascites • Splenomegaly alone (in the absence of other radiological and laboratory findings) is not considered to be a sign of clinically significant portal hypertension and is not an exclusion criterion. 58. HVPG ≥ 12 mmHg (if available historically or if measured at the time of de novo liver biopsy) 59. Liver biopsy characteristics: * F0 in de novo biopsy; Enrollment cap of 20% for F1 in de novo biopsy. * F0 and F1 in historical liver biopsy * Absence of all three components of MASH (steatosis, hepatocyte ballooning, and lobular inflammation) in patients with F1, F2, and F3 * Absence of steatosis (\<5%) in patients with F4 * Diagnosis other than MASH

Treatments Being Tested

PROCEDURE

Metabolic surgery

Patients receive either RYGB or SG. The surgical risk, differential impact of each procedure on body weight and other obesity-related diseases, presence of other medical and mental problems, patient's behavioral factors (e.g., postoperative compliance, active smoking), medications, and goals will be considered when the patient and local medical team make a shared decision about the most appropriate surgical procedure

DRUG

Incretin-Based Therapy

Three incretin-based medications that have been approved for treatment of obesity including liraglutide, semaglutide, or tirzepatide will be used in the nonsurgical group. Any of these 3 medications (in the injection or oral from) based on availability in each country, access, and clinical indications can be used. If possible, patients will be placed on high-dose tirzepatide (Mounjaro or Zepbound 15 mg once weekly injection) or high-dose semaglutide (Wegovy 2.4 mg once weekly injection or Ozempic 2 mg once weekly injection). Other acceptable, less preferrable, options: liraglutide (Saxenda or Victoza), semaglutide tablet (Rybelsus), or lower dose of tirzepatide and semaglutide injections.

Locations (20)

Trial sites listed on ClinicalTrials.gov for this study. Site activation status can vary — confirm with the specific site before traveling for a screening visit.

Banner Health Center
Phoenix, Arizona, United States
Indiana University
Indianapolis, Indiana, United States
Mayo Clinic
Rochester, Minnesota, United States
Cleveland Clinic
Cleveland, Ohio, United States
Hospital Alemão Oswaldo Cruz
São Paulo, Brazil
McGill University
Montreal, Canada
Turku University Hospital
Turku, Finland
Sri Aurobindo Institute of Medical Sciences
Indore, India
The Digestive Health Institute
Mumbai, India
University College Dublin
Dublin, Ireland
Università Cattolica del Sacro Cuore
Milan, Italy
Sapienza Università di Roma
Roma, Italy
Kuwait University
Kuwait City, Kuwait
Instituto Nacional de Ciencias Médicas y Nutrición Salvador
Mexico City, Mexico
Hospital Clínic Barcelona
Barcelona, Spain
Linköping University
Linköping, Sweden
Örebro University
Örebro, Sweden
Clarunis Universitäres
Basel, Switzerland
Hôpitaux universitaires de Genève
Geneva, Switzerland
Nuffield Health Bristol Hospital
Bristol, United Kingdom

How to Talk to Your Doctor About This Trial

Bring the printable summary of this trial — including the NCT ID (NCT06374875), the sponsor (Ali Aminian), and the key eligibility criteria — to your next appointment. Your doctor can review the inclusion and exclusion criteria against your medical history, lab values, and current treatments to assess whether you are likely to qualify. They can also help you weigh whether trial participation makes sense alongside your existing care plan.

Useful questions to walk through together: What does the trial protocol require beyond standard care? How long is the active treatment phase, and how long is follow-up? Are there study visits at sites I can reach? Who pays for the trial-specific procedures, and who pays for standard-of-care portions? See our 25 questions to ask about clinical trials guide for a more complete checklist.

Authoritative Sources

The official record for this trial lives on ClinicalTrials.gov — the federal registry maintained by the National Library of Medicine at NIH. For background on how this trial fits into the FDA approval pathway, see the FDA drug approval process. For oncology-specific guidance for patients considering trials, the National Cancer Institute publishes patient-oriented overviews. International trial registries are aggregated by the WHO ICTRP.

Frequently Asked Questions

What is the NCT06374875 clinical trial studying?

Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly known as non-alcoholic fatty liver disease (NAFLD), a major global public health concern, is commonly associated with obesity, diabetes, and dyslipidemia. MASLD is currently the most common cause of chronic liver disease affecting about 80% of people with obesity, ranging from simple fat deposits in the liver to Metabolic Dysfunction-Associated Steatohepatitis (MASH), cellular injury, advanced fibrosis, cirrhosis, or hepatocellular carcinoma. Patients with MASH are also at risk for cardiovascular disease and mortality. … The full protocol is registered on ClinicalTrials.gov and includes the primary outcome measures, eligibility criteria, and study endpoints.

Who can participate in NCT06374875?

Eligibility for this trial depends on the specific inclusion and exclusion criteria set by the sponsor. The plain-English summary above translates the most important criteria into accessible language; the official clinical text is preserved in the collapsible section underneath. Whether you fit any specific trial is a medical decision your doctor needs to confirm — bring the trial information to your treating physician for a full review against your medical history.

How do I contact the trial site for NCT06374875?

Contact information registered with ClinicalTrials.gov is shown in the sidebar of this page. Before reaching out, confirm with your treating physician that this trial is appropriate for your situation. The trial site will then walk you through the screening process to determine final eligibility.

Is participating in a clinical trial safe?

Clinical trials in the United States are regulated by the FDA and overseen by Institutional Review Boards (IRBs) that review the protocol for safety. Risk varies by trial — Phase 1 studies test new treatments in humans for the first time, while Phase 3 trials use treatments that have already passed earlier safety screening. The informed consent document for any specific trial details the known risks and what to expect. Discuss those risks with your physician before deciding whether to participate.

Where can I verify the data on this page?

Every detail on this page comes directly from the ClinicalTrials.gov API. Click "View on ClinicalTrials.gov" in the sidebar to see the official, unmodified record. The federal record is always authoritative; this page is a structured presentation with a plain-English eligibility translation. For background on how clinical trials are regulated, see the FDA drug approval process documentation.

How This Page Is Built

Every field on this page is pulled directly from the ClinicalTrials.gov API v2 — no estimates, no proxies. The plain-English eligibility translation is generated from the original protocol text and reviewed for fidelity to the underlying clinical criteria. The original clinical text remains visible in the collapsible section above so users and clinicians can verify the translation. Read the full methodology for the data pipeline and known limitations.

Source: ClinicalTrials.gov API v2 record for NCT06374875. Maintained by the National Library of Medicine at NIH. Public domain. Cite as: "TrialFinderData. NCT06374875. Data: ClinicalTrials.gov."

Medical disclaimer: This page is informational, not medical advice. Talk to your doctor about whether a clinical trial is right for you.

Last updated 2026-05-08 · Data from ClinicalTrials.gov.