跳至主要内容
临床试验/NCT02815891
NCT02815891招募中不适用

A Longitudinal Observational Study of Patients With Nonalcoholic Steatohepatitis (NASH) and Related Conditions Across the Entire Spectrum of Nonalcoholic Fatty Liver Disease (NAFLD)

Target PharmaSolutions, Inc.146 个研究点 分布在 1 个国家目标入组 15,000 人开始时间: 2016年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
15,000
试验地点
146
主要终点
Examine liver histology

研究概览

简要总结

TARGET-NASH is a longitudinal observational cohort study of patients being managed for NASH and related conditions across the entire spectrum NAFLD in usual clinical practice. TARGET-NASH is a research registry of patients with NAFL or NASH within academic and community real-world practices maintained in order to assess the safety and effectiveness of current and future therapies.

研究设计

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

入排标准

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

入选标准

  • 1. Adults and children (age 2 or older) being managed or treated for nonalcoholic fatty liver disease. Diagnosis is based on the clinical judgement of the care provider.

排除标准

  • 1. Inability to provide informed assent/consent.

结局指标

主要结局

Examine liver histology

时间窗: 10 years

Estimate adverse event frequency and severity and describe management practices

时间窗: 10 years

NASH can often be an asymptomatic disease in the setting of other disease-related comorbidities such as diabetes and cardiovascular disease. Once NASH progresses to cirrhosis, these patients can suffer the attendant complications of decompensated liver disease including debilitating fatigue, muscle wasting, ascites, bleeding, encephalopathy, hepatocellular carcinoma, and death. NASH therapies may increase the frequency and severity of certain adverse events, such as edema (pioglitazone), some cancers (vitamin E), and new agents or combinations of agents may have their own unique adverse event profiles and varying needs for management plans (e.g., pruritus and dyslipidemia).

Evaluate the impact of NASH therapies on medical co-morbidities

时间窗: 10 years

Establish an understanding of the current natural history of NASH at academic and community medical centers

时间窗: 10 years

A detailed analysis of demographics, concurrent medications, metabolic and cardiovascular co-morbidities, staging of liver disease, and outcomes for patients with NASH managed in diverse clinical settings will serve as an important comparator for subsequent interventions that alter the treatment paradigm for this disease.

Evaluate NASH treatment regimens being used in clinical practice

时间窗: 10 years

Currently, there are no FDA approved therapies for NASH, however clinicians may use a variety of interventions including diet and exercise programs, vitamin E, bariatric surgery or other unapproved uses of some cholesterol, lipid lowering, anti-diabetic and anti-inflammatory medications as well as alternative medications. TARGET-NASH will monitor the safety and effectiveness of the various treatment choices in enrolled patients.

Examine populations underrepresented in phase II-III clinical trials

时间窗: 10 years

Patients with cirrhosis, age \> 70, patients who consume moderate amounts of alcohol and patients with multiple comorbidities such as severe depression, chronic fatigue, fibromyalgia, type 2 diabetes, inflammatory bowel disease, or cardiovascular disease.

Evaluate optimal duration and combination of NASH therapies to achieve clinical response and clinical remission

时间窗: 10 years

In addition to diet and exercise, type, dose and duration of therapy of each NASH treatment (both current unapproved therapies and future FDA approved drugs) will be closely followed, with a goal to monitor treatment paradigms and various combination regimens for clinical response and clinical remission.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (146)

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