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临床试验/NCT04424914
NCT04424914终止不适用

GLOBAL PREVALENCE OF TRANSTHYRETIN AMYLOID CARDIOMYOPATHY (ATTR-CM) IN PARTICIPANTS WITH HEART FAILURE WITH PRESERVED EJECTION FRACTION (HFpEF)

Pfizer100 个研究点 分布在 8 个国家目标入组 347 人开始时间: 2020年12月30日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Pfizer
入组人数
347
试验地点
100
主要终点
Global Prevalence of ATTR-CM in HFpEF Participants Clinically At-Risk of Disease Among Total Evaluable Participants

研究概览

简要总结

This study is a global, multi-center study designed to estimate the global prevalence of transthyretin amyloid cardiomyopathy (ATTR-CM) within a clinically at risk population [participants with heart failure with preserved ejection fraction (HFpEF)].

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

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

入选标准

  • Medical history of heart failure (HF) with:
  • At least 1 episode with clinical evidence of HF (without hospitalization) by signs or symptoms of volume overload or elevated intracardiac pressures that required/requires treatment with a diuretic for improvement; OR
  • 1 prior hospitalization for HF.
  • Left ventricular ejection fraction (LVEF) >40%.
  • End-diastolic interventricular septal wall thickness (IVST) ≥12 mm.
  • Willing and able to undergo scintigraphy.

排除标准

  • Diagnosis of heart failure with reduced ejection fraction (HFrEF) (EF ≤40%).
  • Prior clinical history of myocardial infarction, CABG or multi-vessel obstructive coronary disease (>50% stenosis of ≥2 epicardial coronary arteries).
  • Presence or history of any severe valvular heart disease (obstructive or regurgitant).
  • A confirmed diagnosis of a non-amyloid infiltrative cardiomyopathy (ie, cardiac sarcoidosis, hemochromatosis), muscular dystrophies, cardiomyopathy with reversible causes, hypertrophic obstructive cardiomyopathy with known genetic etiology, or known pericardial constriction.
  • Any type of diagnosed amyloidosis (eg, amyloid A amyloidosis, primary [light chain] amyloidosis) or prior diagnosis of ATTR-CM.

结局指标

主要结局

Global Prevalence of ATTR-CM in HFpEF Participants Clinically At-Risk of Disease Among Total Evaluable Participants

时间窗: Day 1

Global prevalence of ATTR-CM in HFpEF participants was obtained by dividing the number of participants who were diagnosed with ATTR-CM in the study by the total number of HFpEF participants evaluated. Diagnosis of ATTR-CM was defined as: cardiac scintigraphy Grade 1, with confirmation of ATTR by cardiac biopsy; or cardiac scintigraphy Grade 2 or above. Exact 95% confidence intervals for the prevalence estimates were calculated using the method of Clopper and Pearson.

次要结局

  • Number of Participants According to TTR Genotypes Among Participants Diagnosed With ATTR-CM(Day 1)
  • Number of HFpEF Participants With and Without ATTR-CM Based on New York Heart Association (NYHA) Classification(Day 1)
  • Global Prevalence of ATTR-CM in Participants With HFpEF Clinically At-Risk of Disease by Subgroups (Regions, Age, Gender) Among Total Evaluable Participants(Day 1)
  • N-terminal Pro-brain Natriuretic Peptide (NT-proBNP) in Participants With and Without ATTR-CM(Day 1)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (100)

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