Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Linzhi Jianghuang Fufang Huoxue Anshen Capsule for Non-alcoholic Fatty Liver (LJF)

7 de junho de 2026 atualizado por: ZhaoXiang Bian, Hong Kong Baptist University

The Efficacy and Safety of Linzhi Jianghuang Fufang Huoxue Anshen Capsule for Non-alcoholic Fatty Liver: a Randomized, Double-blinded, Placebo-controlled Trial

This is a randomized, double-blinded, placebo-controlled clinical trial aimed at evaluating the efficacy and safety of Linzhi Jianghuang Fufang Huoxue Anshen Capsule (LJF) for non-alcoholic fatty liver.

Visão geral do estudo

Descrição detalhada

Non-alcoholic fatty liver disease (NAFLD), also known as metabolic dysfunction-associated fatty liver disease (MAFLD), refers to a spectrum of conditions characterized by abnormal lipid metabolism leading to fat accumulation within the liver. This spectrum includes non-alcoholic fatty liver (NAFL), non-alcoholic steatohepatitis (NASH), hepatic fibrosis, and cirrhosis.

Linzhi Jianghuang Linzhi Jianghuang Fufang Huoxue Anshen Capsule (LJF) is composed of five herbs (e.g., Salviae Miltiorrhizae Radix et Rhizoma, Puerariae Lobatae Radix). A total of 180 participants aged 18-65 years with Magnetic Resonance Imaging-Proton Density Fat Fraction (MRI-PDFF) ≥ 10% will be recruited and randomized to receive either LJF or placebo in a 1:1 ratio for 24 weeks.

Tipo de estudo

Intervencional

Inscrição (Estimado)

180

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • 1) Age between 18 and 65 years (inclusive);
  • 2) Magnetic Resonance Imaging-Proton Density Fat Fraction (MRI-PDFF) ≥ 10%;
  • 3) Liver stiffness measured by transient elastography < 7.3 kPa;
  • 4) Presence of one or more metabolic risk factors: a. Fasting plasma glucose ≥ 6.1 mmol/L, or 2-hour postprandial glucose ≥ 7.8 mmol/L, or HbA1c ≥ 5.7%, or a history of type 2 diabetes, or HOMA-IR ≥ 2.5; b. Arterial blood pressure ≥ 130/85 mmHg, or receiving antihypertensive medication; c. Fasting serum triglycerides ≥ 1.7 mmol/L;
  • 5) Diagnosis of NAFLD with Phlegm-Stasis Obstructing Collateral pattern according to Traditional Chinese Medicine (TCM) criteria, formulated based on the "Consensus Opinion on Integrated Traditional Chinese and Western Medicine Diagnosis and Treatment of Non-alcoholic Fatty Liver Disease (2017)": Primary Symptoms: a. Intercostal stabbing or dull pain; b. Palpable abdominal mass (hypochondriac mass); c. Dark or dull complexion; d. Obesity. Secondary Symptoms: a. Epigastric and chest fullness and oppression; b. Expectoration of sputum; c. Poor appetite and aversion to greasy food; d. Heavy sensation in the limbs. Tongue and Pulse: Dark red tongue with ecchymosis, enlarged tongue body with teeth marks, greasy coating; wiry, slippery, or hesitant pulse. Diagnosis can be established with the presence of at least 2 primary symptoms and 1 or 2 secondary symptoms, in conjunction with the tongue and pulse presentation.
  • 6) Understand the trial content thoroughly and voluntarily sign the informed consent form.

Exclusion Criteria:

  • 1) Excessive alcohol intake (converted pure alcohol > 210 g per week for men, > 140 g per week for women), or an Alcohol Use Disorder Identification Test (AUDIT) score ≥ 8;
  • 2) Other liver diseases (e.g., alcoholic hepatitis, viral hepatitis, drug-induced liver disease, Wilson's disease, autoimmune liver disease, etc.), or a history of liver transplantation or liver resection;
  • 3) Presence of severe concurrent diseases affecting the heart, brain, hematopoietic system, immune system, or kidneys (BUN > 1.5 × ULN, Cr > ULN);
  • 4) Presence of other endocrine system disorders, such as hyperthyroidism, Cushing's syndrome, etc.;
  • 5) History of malignancy that has not been in complete remission for more than 5 years;
  • 6) Hepatic decompensation (total bilirubin, platelet count, prothrombin time, albumin > ULN; ALT or AST > 2 × ULN), presence of ascites, varices, or a history of hepatic encephalopathy;
  • 7) Poorly controlled severe hypertension, defined as systolic blood pressure ≥ 180 mmHg and/or diastolic blood pressure ≥ 110 mmHg;
  • 8) Insulin-dependent diabetes mellitus (e.g., type 1 diabetes mellitus, or current use of insulin), or non-insulin-dependent diabetes mellitus with poor glycemic control (HbA1c ≥ 9.5%), or diabetic acute complications, or diabetes with severe chronic complications;
  • 9) Use of medications that may cause hepatic steatosis or steatohepatitis (e.g., tamoxifen, amiodarone, glucocorticoids, tetracyclines, methotrexate, valproate, salicylates, estrogens) or potentially hepatotoxic drugs for 2 consecutive weeks or more within the past year;
  • 10) Current use or use within the past 3 months of GLP-1 receptor agonists;
  • 11) Adjustment of hypoglycemic, antihypertensive, or lipid-lowering medications within the past 3 months (e.g., adding or discontinuing medication, dose change, or irregular use);
  • 12) Regular use of hepatoprotective drugs or vitamin E within the past month;
  • 13) History of bariatric surgery within the past year, or body weight change > 5% within the past 3 months;
  • 14) History of surgery within the past month;
  • 15) Coagulation abnormalities, or current use of medications or foods with anticoagulant effects (e.g., aspirin, warfarin, Panax notoginseng, safflower, Angelica sinensis, peach kernel, etc.);
  • 16) Concomitant psychiatric or psychological disorders, or substance/drug abuse;
  • 17) Known allergic constitution, or known allergy to any component of LJF;
  • 18) Participation in another clinical trial within the past month;
  • 19) Contraindications for MRI examination, such as claustrophobia or presence of metallic implants;
  • 20) Individuals of childbearing potential (male or female) with fertility plans; pregnant or lactating women.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: LJF group
Subjects in the LJF group will receive oral LJF capsules, 3 capsules per dose (0.4 g per capsule; total 1.2 g), administered twice daily for a duration of 24 weeks.
Linzhi Jianghuang Fufang Huoxue Anshen Capsule (LJF) is composed of five herbs (e.g., Salviae Miltiorrhizae Radix et Rhizoma, Puerariae Lobatae Radix).
Comparador de Placebo: Placebo group
Subjects in the placebo group will receive placebo capsules, 3 capsules per dose (0.4 g per capsule; total 1.2 g), administered twice daily for a duration of 24 weeks.
The placebo contains caramel color, sucrose octaacetate, sucralose, etc.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
MRI-PDFF
Prazo: Week-0, week-24.
Primary endpoint will be the change in liver fat content from baseline, as measured by Magnetic Resonance Imaging-Proton Density Fat Fraction (MRI-PDFF) after 24 weeks of treatment.
Week-0, week-24.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Liver fat content
Prazo: Week-0, week-12, and week-24.
Changes in liver fat content from baseline, as measured by Liverscan.
Week-0, week-12, and week-24.
Liver stiffness
Prazo: Week-0, week-12, and week-24.
Changes in liver stiffness from baseline, as measured by Liverscan.
Week-0, week-12, and week-24.
Metabolic parameter
Prazo: Week-0, week-24.
Changes in metabolic parameter (e.g., insulin resistance) from baseline to the end of 24 weeks of treatment.
Week-0, week-24.
Anthropometric parameter
Prazo: Week-0, week-12, and week-24.
Changes in anthropometric parameter (e.g., Body Mass Index) from baseline.
Week-0, week-12, and week-24.
Fatty Liver Index
Prazo: Week-0, week-24.
Change in Fatty Liver Index (FLI) score from baseline to the end of 24 weeks of treatment. It ranges from 0 to 100. A FLI < 30 can be used to rule out and a FLI ≥ 60 to rule in hepatic steatosis.
Week-0, week-24.
Hepatic Steatosis Index
Prazo: Week-0, week-24.
Change in Hepatic Steatosis Index (HSI) score from baseline to the end of 24 weeks of treatment. The result is expressed on a scale from 0 to 100, with values <30 ruling out fatty liver, whereas values >36 confirm its presence.
Week-0, week-24.
Fibrosis-4 Index
Prazo: Week-0, week-24.
Change in Fibrosis-4 Index (FIB-4) score from baseline to the end of 24 weeks of treatment. A FIB-4 score below 1.30 generally indicates a low likelihood of liver fibrosis.
Week-0, week-24.
CLDQ-NAFLD
Prazo: Week-0, week-12, and week-24.
Changes in the Chronic Liver Disease Questionnaire-Non-Alcoholic Fatty Liver Disease (CLDQ-NAFLD) score. Each item is scored on a 7-point Likert scale, and the total score is the average of the 6 domain scores, with higher scores indicating better quality of life.
Week-0, week-12, and week-24.
Sleep quality
Prazo: Week-0, week-12, and week-24.
Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI), a 19-item instrument whose items generate 7 component scores that are summed into a global score ranging from 0 to 21, with higher scores indicating poorer sleep quality.
Week-0, week-12, and week-24.
Fatigue
Prazo: Week-0, week-12, and week-24.
Fatigue will be assessed using the Chalder Fatigue Questionnaire (CFQ-11), an 11-item instrument whose scores are summed into a total score ranging from 0 to 33, with higher scores indicating greater fatigue.
Week-0, week-12, and week-24.
Adverse events
Prazo: From week-0 to week-24
Adverse events (AEs) occurring from the participant's enrollment to the end of the trial and any abnormal changes in laboratory parameters will be recorded.
From week-0 to week-24

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Dietary intake
Prazo: Week-0, week-12, and week-24.
Dietary intake will be assessed using a validated Food Frequency Questionnaire (FFQ).
Week-0, week-12, and week-24.
Physical activity
Prazo: Week-0, week-12, and week-24.
Physical activity (e.g., step count) as measured by a smartwatch.
Week-0, week-12, and week-24.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de setembro de 2026

Conclusão Primária (Estimado)

1 de julho de 2028

Conclusão do estudo (Estimado)

1 de janeiro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

28 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

7 de junho de 2026

Primeira postagem (Real)

9 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

9 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

7 de junho de 2026

Última verificação

1 de março de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever