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临床试验/NCT06358196
NCT06358196尚未招募不适用

Complex Exploratory Study of Alcohol-Associated Hepatitis

Pavol Jozef Safarik University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Standardized annual incidence of (severe) alcoholic hepatitis in the Kosice Urban Area

研究概览

简要总结

Alcohol-associated hepatitis is a clinical syndrome distinct from steatohepatitis or liver cirrhosis. It is associated with high mortality and characterized by an absence of effective treatment, while corticosteroids, which are currently used as the first-line treatment are effective only in a subpopulation of patients and only on 28-days survival - their effect on survival does not last beyond this interval. The proposed study is a complex exploratory study of alcohol-associated hepatitis with several epidemiology- and prognosis-related aims.

详细描述

Alcohol-associated hepatitis is a clinical syndrome distinct from steatohepatitis or liver cirrhosis. It is associated with high mortality and characterized by an absence of effective treatment, while corticosteroids, which are currently used as the first-line treatment are effective only in a subpopulation of patients and only on 28-days survival - their effect on survival does not last beyond this interval. The proposed study is a complex exploratory study of alcohol-associated hepatitis with the following aims: (1) to estimate the standardized annual incidence of (severe) AH in the Kosice Urban Area, (2) to estimate the threshold of alcohol consumption associated with (an increased risk of) developing AH, (3) to compare the diagnostic accuracy of NIAAA vs NIAAAm-CRP against liver biopsy, (4) to perform a head-to-head comparison of widely-accepted prognostic models and to develop prognostic models, (5) to observe prognosis of nonsevere alcohol-associated hepatitis, (6) to observe the evolution of severe alcohol-associated hepatitis, (7) to describe the association of hypothalamus-hypopituitary-adrenal axis and Gut-Liver Microbiome Axis and Prognosis of Alcohol-associated Hepatitis, (8) to describe the adherence to outpatient psychiatric management and its impact on long-term prognosis, (9) to perform a longitudinal evaluation of nutritional status, its changes, and its impact on long-term prognosis.

Study Design This is a multicenter observational study of patients with alcohol-associated hepatitis. The total trial duration for each subject is approximately 53 weeks. This includes a screening period of a maximum of one week (7 days), during which the diagnosis of AH will be confirmed, followed by a 52 weeks (365 days) observational period.

Diagnosis of Alcohol-associated Hepatitis The diagnosis of alcohol-associated hepatitis will be established using the National Institute on Alcohol Abuse and Alcoholism (NIAAA) diagnostic criteria: onset of jaundice within prior 8 weeks; ongoing consumption of >40 (females) or >60 (males) g alcohol/day ≥ 6 months, with less than 60 days of abstinence before the onset of jaundice; aspartate aminotransferase >0.83µkat/L (but less than 6.64 µkat/L), AST/ALT > 1.5, and total serum bilirubin > 51.3 mmol/L.

NIAAA definitions for AH differentiate between possible AH (clinically diagnosed with potential confounding factors), in which transjugular liver biopsy is indicated, probable AH (clinically diagnosed without potential confounding factors), and definite AH (clinically diagnosed and biopsy proven).

Considerations Regarding Patient Admission and Discharge Local standards dictate that patients with acute liver injury or acute liver failure are typically admitted to the 2nd Department of Internal Medicine, which specializes in gastroenterology and hepatology. This admission is carried out to facilitate further differentiation and provide specific treatment tailored to their condition. However, patients have the option to decline admission and, in such cases, will be discharged and managed as outpatients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patients older than 18 years with acute liver injury / acute liver failure with later confirmation of the AH diagnosis according to the NIAAA diagnostic criteria [14] who provided written informed consents for admission and further differentiation, and for study participation

排除标准

  • Patients not confirmed to have alcohol-associated hepatitis
  • Patients with malignancies (specifically those with life-expectancy limitation)
  • Patients who withdrew consent for study participation

结局指标

主要结局

Standardized annual incidence of (severe) alcoholic hepatitis in the Kosice Urban Area

时间窗: 1 year

Number of patients with (severe) alcoholic hepatitis

次要结局

  • Uper limit of MELD or Maddrey scores beyond which patients no longer derive any therapeutic benefit from corticosteroid treatment(Baseline)
  • Prognostic model for 90 day survival(Baseline)
  • An update of Maddrey, MELD, MELD-Na, MELD 3.0, GAHS, ABIC, Lille score(Baseline)
  • Diagnostic accuracy of NIAAA and NIAAAm-CRP(Baseline)
  • Prognostic performance of Maddrey, MELD, MELD-Na, MELD 3.0, GAHS, ABIC, Lille score(Baseline, Days 2, 4, 7)
  • Natural course of nonsevere alcoholic hepatitis(1 year)
  • Natural course of severe alcoholic hepatitis(1 year)
  • Risk score for bacterial infection before corticosteroid treatment in patients with alcoholic hepatitis(Baseline)
  • GUT microbiome and treatment response in alcoholic hepatitis(Baseline, Day 90)
  • Threshold of alcohol consumption associated with (an increased risk of) developing AH(Baseline)
  • Prognostic performance of SOFA and CLIF-C(Baseline, Days 2, 4, 7)
  • Alternative to Lille model(Baseline, Day 2)
  • Distinguishing sterile Inflammation from infection in alcoholic hepatitis(1 year)
  • Hypothalamus-pituitary-adrenal axis and treatment response in alcoholic hepatitis(Baseline, Day 28)
  • Adherence to outpatient psychiatric management(1 year)
  • Nutritional status and treatment response in alcoholic hepatitis(Baseline)

研究者

发起方
Pavol Jozef Safarik University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jakub Gazda

Principial Investigator

Pavol Jozef Safarik University

研究点 (1)

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