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Impact of Ganoderma Lucidum on NRF2 Levels and Antioxidant Status in Metabolic Asscociated Fatty Liver Disease (GL-MAFLD-NRF2 Study) (GL-MAFLD-NFR2)

2026年4月27日 更新者:Kalsoom Siddiq、University of Agriculture, Peshawar

Impatc of Ganoderma Lucidum on NRF2 Levels and Antioxidant Status in Metabolic Asscociated Fatty Liver Disease

This RCT investigates the impact of Ganoderma lucidum on antioxidant staus, NRF2 levels and lipid metabolism in individuals with Metabolic Associated Fatty Liver Disease.

研究概览

详细说明

The prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing worldwide. Unfortunately, for the treatment of NAFLD no FDA-approved drugs are available currently. Therefore, natural products are currently used as alternative treatments for fatty liver disease. Ganoderma lucidum is a traditional, medicinal edible mushroom with significant health benefits. It contains bioactive compounds such as polysaccharides, polyphenols and triterpenoids which have significant antioxidant, anti-inflammatory and anti-cancer properties.

Previous studies have shown the protective effect of GL extract against cancer, diabetes and hepatotoxicity. However, limited evidence is available on the specific interaction of these compounds with Nrf2 pathway a key regulator of cellular redox balance and detoxification has not been extensively studied. Therefore, the present study aims to investigate the effect of GL extract on the Nrf2 pathway in human experimental models.

By elucidating the molecular mechanisms involved, this study could pave the way for the development of new, natural, and effective interventions for a variety of chronic diseases driven by oxidative stress and inflammation. Moreover, the findings may contribute to the broader field of nutraceutical and their role in supporting health at the cellular level.

Previous studies in animal models have shown the potential lipid lowering mechanism of GLP. However, few human intervention studies have been conducted on the effect of GL on lipid lowering pathways in humans. Therefore, the present study aims to investigate the effect of GL on lipid lowering mechanisms in human studies.

This study will provide new knowledge on the potential for the mushroom extract on liver, inflammatory and oxidative stress biomarkers that may be of benefit for the prevention and control of non-alcoholic fatty liver.

研究类型

介入性

注册 (估计的)

40

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Khyber Pakhtunkhwa
      • Peshawar、Khyber Pakhtunkhwa、巴基斯坦、25120
        • The University of Agriculture, Peshawar

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Adults aged 35-49 years.
  • Stage 1 and 2 fatty liver
  • Lipid profile test markers (elevated LDL, total cholesterol, or triglycerides less than 150mg/dL high 200-499mg/dL and 500 mg/dL are above high.
  • Liver function test markers, ALT > 56 U/L, AST>40 U/L, ALP>147 UL.
  • Inflammatory markers:TNF-α ≥8 pg/mL

Exclusion Criteria:

  • Participants having diabetes, psychological illness or depression, renal or cardiac disease, or other physiological conditions such as pregnancy, breastfeeding, or a history of stroke will excluded from this research.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:Starch
Starch will be used as placebo comparator.
Intervention will invovle the the intake of Starch Placebo capsule
实验性的:Intervention
Ganoderma lucidum mushroom powder will be used as experimental capsule.Each capsule contains 1000 mg of mushroom dried powder
Intervention will involve the intake of Ganoderma lucidum mushroom powder

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Plasma Total Antioxidant Capacity (T-AOC)
大体时间:Baseline (day one) - 12 week & 24 weeks
Plasma Total Antioxidant Capacity (T-AOC) will be measured to determined the antioxidative effect of ganoderma mushroom in participants with fatty liver.
Baseline (day one) - 12 week & 24 weeks

次要结果测量

结果测量
措施说明
大体时间
LFTs
大体时间:Baseline (day one) - 12 weeks & 24 weeks (endline)
Liver Function Test inclusing ALT, AST and ALP will be mesuare.
Baseline (day one) - 12 weeks & 24 weeks (endline)
Lipid Profile
大体时间:Baseline (day one) - 12 weeks & 24 weeks (endline)
Lipid profile including LDL-C, HDL-C, triglycerides will be estimated.
Baseline (day one) - 12 weeks & 24 weeks (endline)
NRF2 Protein levels
大体时间:Baseline (day one) - 12 weeks & 24 weeks (endline)
NRF2 Protein levels will be meausred as key regulator of cellular redox and detoxification balance.
Baseline (day one) - 12 weeks & 24 weeks (endline)
TNF-alpha
大体时间:Basline (day one)- 12 weeks & 24 weeks
TNF-alpha will measured as marker of inflmmation.
Basline (day one)- 12 weeks & 24 weeks
Abdominal Ultrasound
大体时间:Basline (day one) - 12 weeks & 24 weeks
Abdominal Ultrasound to asses fat acculumation in liver.
Basline (day one) - 12 weeks & 24 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Bibi Hajira, PhD、Khyber Medical University Peshawar

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年4月28日

初级完成 (估计的)

2027年4月20日

研究完成 (估计的)

2027年4月20日

研究注册日期

首次提交

2026年4月27日

首先提交符合 QC 标准的

2026年4月27日

首次发布 (实际的)

2026年5月4日

研究记录更新

最后更新发布 (实际的)

2026年5月4日

上次提交的符合 QC 标准的更新

2026年4月27日

最后验证

2026年4月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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