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- Klinische proef 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
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
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.
Studietype
Inschrijving (Geschat)
Fase
- Fase 2
Contacten en locaties
Studiecontact
- Naam: Jialing ZHANG, PhD
- Telefoonnummer: 852-34115024
- E-mail: zhangjialing@hkbu.edu.hk
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: 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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Placebo-vergelijker: 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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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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MRI-PDFF
Tijdsspanne: Week-0, week-24.
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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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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Liver fat content
Tijdsspanne: Week-0, week-12, and week-24.
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Changes in liver fat content from baseline, as measured by Liverscan.
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Week-0, week-12, and week-24.
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Liver stiffness
Tijdsspanne: Week-0, week-12, and week-24.
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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
Tijdsspanne: Week-0, week-24.
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Changes in metabolic parameter (e.g., insulin resistance) from baseline to the end of 24 weeks of treatment.
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Week-0, week-24.
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Anthropometric parameter
Tijdsspanne: Week-0, week-12, and week-24.
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Changes in anthropometric parameter (e.g., Body Mass Index) from baseline.
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Week-0, week-12, and week-24.
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Fatty Liver Index
Tijdsspanne: Week-0, week-24.
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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
Tijdsspanne: Week-0, week-24.
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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.
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Week-0, week-24.
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Fibrosis-4 Index
Tijdsspanne: Week-0, week-24.
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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.
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Week-0, week-24.
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CLDQ-NAFLD
Tijdsspanne: Week-0, week-12, and week-24.
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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
Tijdsspanne: Week-0, week-12, and week-24.
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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
Tijdsspanne: Week-0, week-12, and week-24.
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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
Tijdsspanne: From week-0 to week-24
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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.
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From week-0 to week-24
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Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Dietary intake
Tijdsspanne: Week-0, week-12, and week-24.
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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
Tijdsspanne: Week-0, week-12, and week-24.
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Physical activity (e.g., step count) as measured by a smartwatch.
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Week-0, week-12, and week-24.
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Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- REC/25-26/0489
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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