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临床试验/NCT01572077
NCT01572077已完成不适用

Rt Ventricular Substrate Metabolism as a Predictor of Rt Heart Failure in Patients With Pulmonary Arterial Hypertension

Ottawa Heart Institute Research Corporation1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2011年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
Cardiopulmonary death OR clinical right heart failure hospitalization

研究概览

简要总结

The purpose of this study is to evaluate patterns of metabolic activity in the heart of patients with pulmonary arterial hypertension(PAH). Patients with PAH are at risk of developing weakness or failure of the right side of the heart.It is possible that there is a relationship between the development of heart failure and the way the heart uses energy sources, such as sugar. This study is designed to evaluate the way the heart uses sugar uptake in patients with PAH using positron emission tomography(PET imaging)

详细描述

PAH results in premature death as a result of right ventricular dysfunction. However, there are substantial differences among patients in their tendency to develop right heart failure. This study proposes to determine if right ventricular (RV) changes can predict the development of right heart failure in patients with PAH.

In addition, the study aims to evaluate the relationship of right ventricular metabolism to other physiologic responses in PAH,including:pulmonary vascular resistance, serum BNP and changes in cardiac hypertrophy and function. In conjunction with hemodynamic measurements, biomarkers and cardiac magnetic resonance imaging (MRI); RV metabolism will be evaluated with (18F) FTHA and (18F)FDG cardiac PET imaging.

A cohort of 20 age sex matched individuals will serve as normal controls. These subjects will have no known cardiac or pulmonary disease with normal ventricular function and estimates pulmonary pressures on echocardiogram.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

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

入选标准

  • •Patients with diagnosis of Category 1 pulmonary arterial hypertension due to any of the following: idiopathic, familial, associated with connective tissue disease, HIV disease or anorexigen use.
  • •All patients who will require a right heart catheterization for further clinical management and/or diagnosis.
  • •Patients will be considered eligible if they have no significant coronary artery disease (stenosis > 70% in a proximal or mid major coronary artery) or moderate coronary artery disease (60-70%) with abnormal left ventricular function (EF<50%)
  • •Patients will be considered eligible in the absence of current or recent evidence of right heart failure.
  • •No previous hospital admission or requirements of intravenous diuretics for right heart failure within 6 months of enrolment.
  • •No increase in oral diuretics to control fluid volume within 6 months prior to enrolment
  • •No current symptoms and signs of fluid retention or right heart strain, including any of the following: development of new ascites or peripheral edema > = 2+, JVP >7 cm above the sternal angle or a right atrial pressure >14 mmHg at the time of right heart catheterization.
  • •In addition, we will include a small cohort of up to 15 patients with PAH and current RHF.

排除标准

  • •Patients with known significant coronary artery disease(defined as known stenosis >70% in a proximal or mid major artery or moderate coronary artery disease (60-70%)in a coronary artery and associated left ventricular ejection fraction <50%.
  • •Patients with diabetes mellitus who require the use of oral hypoglycemics and or insulin.
  • •Implantable metal devices, incompatible with magnetic resonance imaging.
  • •Other contraindications of magnetic resonance imaging.
  • •Normal Control Subjects:
  • •Subjects will have no known cardiac or pulmonary disease.
  • •Normal ventricular function and estimated pulmonary pressures on echocardiogram.

研究组 & 干预措施

FTHA/GDF PET imaging

Experimental

This study plans to enrol 60 subjects with Type I pulmonary arterial hypertension (PAH) and 20 healthy, age and sex individuals to serve as normal controls. These subjects will have no known cardiac or pulmonary disease.

Both groups will undergo FTHA/FDG PET imaging.

干预措施: FTHA, FDG PET imaging. (Radiation)

结局指标

主要结局

Cardiopulmonary death OR clinical right heart failure hospitalization

时间窗: 1year

Clinical RHF admission requiring ONE of the following:intravenous diuretics or an increase in oral diuretics \>50%of baseline for at least 7 days.

次要结局

  • Change in right ventricular size and function as measured by cardiac MRI, between baseline and 1 year.(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lisa Mielniczuk

Co- Medical Director Pulmonary Hypertension Clinic

Ottawa Heart Institute Research Corporation

研究点 (1)

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