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- Ensayo clínico NCT07637006
Linzhi Jianghuang Fufang Huoxue Anshen Capsule for Non-alcoholic Fatty Liver (LJF)
The Efficacy and Safety of Linzhi Jianghuang Fufang Huoxue Anshen Capsule for Non-alcoholic Fatty Liver: a Randomized, Double-blinded, Placebo-controlled Trial
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
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 estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Jialing ZHANG, PhD
- Número de teléfono: 852-34115024
- Correo electrónico: zhangjialing@hkbu.edu.hk
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
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.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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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.
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Linzhi Jianghuang Fufang Huoxue Anshen Capsule (LJF) is composed of five herbs (e.g., Salviae Miltiorrhizae Radix et Rhizoma, Puerariae Lobatae Radix).
|
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Comparador de placebos: 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.
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The placebo contains caramel color, sucrose octaacetate, sucralose, etc.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
MRI-PDFF
Periodo de tiempo: 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.
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Week-0, week-24.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Liver fat content
Periodo de tiempo: 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.
|
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Liver stiffness
Periodo de tiempo: Week-0, week-12, and week-24.
|
Changes in liver stiffness from baseline, as measured by Liverscan.
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Week-0, week-12, and week-24.
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Metabolic parameter
Periodo de tiempo: 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.
|
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Anthropometric parameter
Periodo de tiempo: 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
Periodo de tiempo: 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.
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Week-0, week-24.
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Hepatic Steatosis Index
Periodo de tiempo: 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.
|
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Fibrosis-4 Index
Periodo de tiempo: 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.
|
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CLDQ-NAFLD
Periodo de tiempo: 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.
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Week-0, week-12, and week-24.
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Sleep quality
Periodo de tiempo: 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.
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Week-0, week-12, and week-24.
|
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Fatigue
Periodo de tiempo: 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.
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Week-0, week-12, and week-24.
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Adverse events
Periodo de tiempo: 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
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Dietary intake
Periodo de tiempo: Week-0, week-12, and week-24.
|
Dietary intake will be assessed using a validated Food Frequency Questionnaire (FFQ).
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Week-0, week-12, and week-24.
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Physical activity
Periodo de tiempo: 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.
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- REC/25-26/0489
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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