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

2026年6月7日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

180

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
実験的: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).
プラセボコンパレーター: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
MRI-PDFF
時間枠: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.

二次結果の測定

結果測定
メジャーの説明
時間枠
Liver fat content
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

その他の成果指標

結果測定
メジャーの説明
時間枠
Dietary intake
時間枠: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
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2028年7月1日

研究の完了 (推定)

2029年1月1日

試験登録日

最初に提出

2026年5月28日

QC基準を満たした最初の提出物

2026年6月7日

最初の投稿 (実際)

2026年6月9日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月9日

QC基準を満たした最後の更新が送信されました

2026年6月7日

最終確認日

2026年3月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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