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临床试验/NCT06135584
NCT06135584尚未招募不适用

Prospective Cohort Study on MAFLD-related Cirrhosis Prevention and Treatment Strategies

The Affiliated Hospital of Hangzhou Normal University0 个研究点目标入组 1,000 人开始时间: 2023年11月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,000
主要终点
Prevalence of cirrhosis

研究概览

简要总结

To establish a prospective, multicenter, biopsie-confirmed clinical cohort of MAFLD-related cirrhosis (F3-F4) in China, and analyze the clinical, histopathological features and natural outcomes of MAFLD-associated liver fibrosis/cirrhosis in China. And than to conducted a real-world study of different strategies of Chinese characteristics for the prevention and treatment of MAFLD-related cirrhosis to evaluate the efficacy and safety of the strategies.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-75 years old, gender and ethnicity are not limited;
  • Meet the diagnostic criteria for MAFLD;
  • F0-F4 stage of liver fibrosis confirmed by liver biopsy within 24 weeks;
  • Be willing to sign informed consent.

排除标准

  • Cirrhosis due to any chronic liver disease other than MAFLD (including but not limited to alcohol or drug abuse, medications, chronic hepatitis B or C, autoimmune, hemochromatosis, Wilson's disease, alpha1-antitrypsin deficiency);
  • Any clinical evidence or history of peritonitis, varicose bleeding, or spontaneous encephalopathy;
  • According to the investigators' assessment, a history of heavy drinking for more than 3 months continuously within the previous year was selected. (Note: Heavy drinking was defined as more than 20 g per day on average for female subjects and more than 30 g per day for male subjects).
  • Use of NAFLD-related medication history (amiodarone, methotrexate, systemic glucocorticoids, tetracycline, tamoxifen, larger than hormone replacement doses of estrogen, anabolic steroids, valproic acid, and other known hepatotoxins) for more than 2 weeks within the year prior to screening.

研究组 & 干预措施

Pioglitazone metformin tablets

Experimental

Pioglitazone metformin tablets 15mg/500mg (To control the fasting blood glucose below 7.0mmol/l, adjust the dose and dosage according to the blood glucose)

干预措施: Pioglitazone metformin tablets (Drug)

Other drug

Active Comparator

Chinese patent medicine or Hypoglycemic drugs other than pioglitazone metformin tablets, pioglitazone, metformin and GLP1 ((To control the fasting blood glucose below 7.0mmol/l)

干预措施: Other drugs (Drug)

Drug-free

Other

Drug-free

干预措施: Drug-free (Other)

结局指标

主要结局

Prevalence of cirrhosis

时间窗: Through study completion, an average of 96 week.

Prevalence of liver transplantation

时间窗: Through study completion, an average of 96 week.

Controlled attenuation parameter (CAP)

时间窗: Through study completion, an average of 96 week.

Transient elastography

时间窗: Through study completion, an average of 96 week.

Model for end-stage liver disease score

时间窗: Through study completion, an average of 96 week.

Model for end-stage liver disease score ranges from 6 to 40 score (\>40 calculated as 40 scores),higher scores mean a worse outcome

Portalvein pressure gradient(HVPG)

时间窗: Through study completion, an average of 96 week.

Prevalence of decompensated cirrhosis

时间窗: Through study completion, an average of 96 week.

次要结局

未报告次要终点

研究者

发起方
The Affiliated Hospital of Hangzhou Normal University
申办方类型
Other
责任方
Sponsor

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