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Идёт набор NCT07400367

Impact of a Probiotic Supplementation With Lifestyle Modification on Liver Steatosis, Fibrosis, and Metabolic Health in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Без фазы С лечением Liver Elastography Liver Steatosis Liver Function Test Insulin Resistance

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Probiotic product, Life style modification, placebo.
Кому может быть актуально
Состояния в реестре: Liver Elastography, Liver Steatosis, Liver Function Test, Insulin Resistance. Базовые параметры: 18 лет — 80 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Тайвань
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Impact of a Multi-strain Probiotic Supplementation With Lifestyle Modification on Liver Steatosis, Fibrosis, and Metabolic Health in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Обзор

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) is the new clinical term introduced in 2023 to redefine what was formerly known as Non-Alcoholic Fatty Liver Disease (NAFLD). It is defined as fatty liver confirmed by imaging or biopsy, accompanied by at least one cardiometabolic risk factor (e.g., hyperglycemia, dyslipidemia, hypertension, or obesity). Its pathological progression ranges from simple steatosis to steatohepatitis, primarily driven by excessive energy intake, hepatic lipid accumulation, and insulin resistance. MASLD is currently the most prevalent chronic liver disease globally, with a prevalence rate of approximately 30-40%. However, there is no satisfactory pharmacological treatment, leaving lifestyle modification as the primary therapeutic approach. Many patients struggle to effectively adjust their habits, leading to persistent hepatic inflammation and damage, which may eventually progress to end-stage diseases such as cirrhosis and hepatocellular carcinoma. In many developed countries, MASLD has become the leading indication for liver transplantation, imposing a heavy burden on healthcare systems. Gut dysbiosis is closely linked to MASLD. An imbalance in the gut microbiota disrupts the gut-liver axis, leading to impaired intestinal mucosal barrier function. This allows bacterial components to enter the circulation, further triggering hepatic inflammation and abnormal lipid metabolism. Consequently, modulating the gut microbiota is considered a potential therapeutic strategy. Over the past decade, probiotics, prebiotics, and synbiotics have been extensively studied as non-pharmacological treatments for NAFLD. Multiple studies indicate that these products can reduce liver enzymes (AST, ALT), insulin resistance (HOMA-IR), and inflammatory markers (hs-CRP, TNF-α). The most effective combinations typically involve Lactobacillus, Bifidobacterium, and Streptococcus, with a recommended duration of approximately 12 weeks. However, the impact of these products on liver fibrosis, hepatic fat accumulation, and cardiometabolic risk factors remains inconclusive. The probiotic product to be tested consists of Lactobacillus salivarius AP-32, Lactobacillus rhamnosus bv-77, Bifidobacterium animalis CP-9, and Lactobacillus reuteri GL-104. This formulation complies with food safety regulations. In clinical studies, it had been proven as an effective adjuvant method that increased beneficial gut bacteria such as Akkermansia muciniphila and improved the control of blood glucose, lipids, and inflammatory markers. Study Objectives This study aims to investigate the efficacy of this probiotic product as an adjuvant therapy alongside lifestyle modifications in adult patients with MASLD. We will evaluate its impact on: 1. The degree of liver fibrosis and steatosis 2. Cardiometabolic risk factors (BMI, waist circumference, blood lipids, and blood glucose). 3. Inflammatory markers. 4. Gut microbiota composition.

Вмешательства

  • Пищевая добавка Probiotic product
    The probiotic product contains Lactobacillus salivarius AP-32, Lactobacillus rhamnosus bv-77, Bifidobacterium animalis CP-9 and Lactobacillus reuteri GL-104
  • Поведенческое Life style modification
    Life style modification of MASLD provided by an gastroenterologist in an outpatient s
  • Пищевая добавка placebo
    placebo sachet looked and taste very similar to the probiotic product being tested

Первичные конечные точки

  • Change in shear wave elastography (m/s) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
Вторичные конечные точки (12)
  • Change in ultrasound attenuation coefficient (dB/cm/MHz) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood LDL level (mg/dL) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood HDL level (mg/dL) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood total cholesterol level (mg/dL) at 12 weeks [Срок оценки: Time Frame: From enrollment to the end of treatment at 12 weeks]
  • Change in blood triglycerides level (mg/dL) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in HOMA-IR at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood fasting insulin level (μU/mL) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood fasting glucose level (mg/dL) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood AST level (U/L) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood ALT level (U/L) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood gamma-GT level (U/L) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Change in blood alkaline phosphatase level (IU/L) at 12 weeks [Срок оценки: From enrollment to the end of treatment at 12 weeks]

Критерии участия

Критерии включения

  • ALT ≥ 60 U/L
  • Liver steatosis identified by ultrasound
  • Meet at least one cardiometabolic criteria:
  • BMI ≥ 25 kg/m2 (Asian ≥23)
  • Waist circumference: > 94cm (M) 80cm(F)
  • Fasting blood glucose ≥ 100 mg/dL
  • HbA1c ≥ 5.7
  • Receiving treatment of diabetes
  • Receiving treatment of Hypertension
  • Average home blood pressure: ≥ 130/85 mmHg
  • TG ≥ 150 mg/dL
  • HDL ≤ 40 mg/dL
  • Receiving treatment of dyslipidemia

Критерии исключения

  • HBsAg(+)
  • Anti-HCV (+)
  • Cirrhosis
  • Excessive alcohol intake ( Male over 210g/wk; Female over 140mg/wk)
  • Could not rule out Autoimmune hepatitis (ANA, or AMA or ASMA (+))
  • Could not rule out drug related hepatitis
  • Receiving drug that might induce liver steatosis:
  • Glucocorticoids
  • Amiodarone
  • Tamoxifen
  • Methotrexate
  • Valproate
  • Tetracycline
  • Chemotherapeutic agents
  • Receiving immune modulators or biologics
  • Receiving antibiotics within 1 month
  • Receiving any cancer treatment
  • Have diagnosis of "Catastrophic Illness" defined by Health Administration of Taiwan
  • eGFR<60
  • Pregnancy
  • Currently enrolled in other dietary or pharmacology clinical trial

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Четверное слепое
Основная цель
Лечение

Центры проведения

Тайвань · 2 центра
  • Fu Jen Catholic University Hospital — New Taipei City
  • Fu Jen Catholic University Hospital — New Taipei City

Публикации

  • Abhari K, Saadati S, Yari Z, Hosseini H, Hedayati M, Abhari S, Alavian SM, Hekmatdoost A. The effects of Bacillus coagulans supplementation in patients with non-alcoholic fatty liver disease: A randomized, placebo-controlled, clinical trial. Clin Nutr ESPEN. 2020 Oct;39:53-60. doi: 10.1016/j.clnesp.2020.06.020. Epub 2020 Jul 24. PMID 32859329
  • Inoue K, Tsukuda S, Kayano H, Tanaka J, Heshiki A. A case of hypervascular renal capsule leiomyoma. Radiat Med. 2000 Sep-Oct;18(5):323-6. PMID 11128405
  • Kumada T, Toyoda H, Ogawa S, Gotoh T, Yoshida Y, Yamahira M, Hirooka M, Koizumi Y, Hiasa Y, Tamai T, Kuromatsu R, Matsuzaki T, Suehiro T, Kamada Y, Sumida Y, Tanaka J, Shimizu M. Diagnostic performance of shear wave measurement in the detection of hepatic fibrosis: A multicenter prospective study. Hepatol Res. 2024 Sep;54(9):851-858. doi: 10.1111/hepr.14026. Epub 2024 Feb 13. PMID 38349813
  • Farrow A, Farrow SC, Little R, Golding J. The repeatability of self-reported exposure after miscarriage. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood. Int J Epidemiol. 1996 Aug;25(4):797-806. doi: 10.1093/ije/25.4.797. PMID 8921459
  • Jansson JH, Boman K, Brannstrom M, Nilsson TK. High concentration of thrombomodulin in plasma is associated with hemorrhage: a prospective study in patients receiving long-term anticoagulant treatment. Circulation. 1997 Nov 4;96(9):2938-43. doi: 10.1161/01.cir.96.9.2938. PMID 9386160
  • Yang Y, Yang L, Wu J, Hu J, Wan M, Bie J, Li J, Pan D, Sun G, Yang C. Optimal probiotic combinations for treating nonalcoholic fatty liver disease: A systematic review and network meta-analysis. Clin Nutr. 2024 Jun;43(6):1224-1239. doi: 10.1016/j.clnu.2024.04.004. Epub 2024 Apr 13. PMID 38643738
  • Wu J, Chen X, Qian J, Li G. Clinical improvement effect of regulating gut microbiota on metabolic dysfunction-associated steatotic liver disease: Systematic review and meta-analysis of randomized controlled trials. Clin Res Hepatol Gastroenterol. 2024 Aug;48(7):102397. doi: 10.1016/j.clinre.2024.102397. Epub 2024 Jun 13. PMID 38879003
  • Sharma S, Tiwari N, Tanwar SS. The current findings on the gut-liver axis and the molecular basis of NAFLD/NASH associated with gut microbiome dysbiosis. Naunyn Schmiedebergs Arch Pharmacol. 2025 Sep;398(9):11541-11579. doi: 10.1007/s00210-025-04069-z. Epub 2025 Apr 9. PMID 40202676

Идентификаторы

NCT: NCT07400367 · FJUH114502

Первоисточники (государственные реестры)

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