跳至主要内容
临床试验/NCT00756379
NCT00756379进行中(未招募)不适用

Randomized Trial of Comprehensive Lifestyle Modifications, Optimal Pharmacological Treatment and PET Imaging for Detection and Management of Stable Coronary Artery Disease

The University of Texas Health Science Center, Houston1 个研究点 分布在 1 个国家目标入组 1,085 人开始时间: 2009年3月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,085
试验地点
1
主要终点
1.Clinical Endpoints-

研究概览

简要总结

The Century Trial is a single center Phase III randomized study sponsored by the Albert Weatherhead III Foundation and conducted by Dr. K. Lance Gould. The study hypothesis is that a combined image-treatment regimen of PET + comprehensive program of lifestyle modification and lipid lowering drugs to target lipid level will result in an improved cardiovascular risk score when compared to current standard optimal medical therapy, potentially resulting in a lower rate of death, non-fatal myocardial infarction (MI) and revascularization procedures during long term follow-up when compared with current standard of care. If our hypothesis is correct, we will not only improve our ability to prevent and treat CAD but we will also illustrate that, even with the expenses of behavioral interventions and imaging techniques, we can be very cost effective. This information may help patients at risk or with known CAD to obtain insurance coverage to prevent the disease as well as providing a more effective way of treating it.

详细描述

Advances in diagnostic imaging with expensive technologies and reimbursement policies that favor illness intervention rather than primary and secondary prevention have resulted in rising costs of health care and more people being deprived of its benefits (Sultz 2004, Bodenheimer 2002).

In the field of coronary artery disease (CAD) are several non-invasive imaging techniques for diagnostic and risk stratification purposes such as echocardiography, perfusion imaging (cardiac stress SPECT - single photon emission computed tomography - and stress PET - positron emission tomography), non-invasive cardiac computed tomography angiography (CTA) and combined perfusion-anatomy (PET-CT) studies. There are an estimated 40 million noninvasive cardiac tests performed each year (Mark DB 2003). For echocardiography and SPECT imaging, reimbursement from Medicare encompasses approximately 30% of all payments, totaling over $1 billion in the year 2000 (ACC 2003). There are, however, basic questions about cardiovascular imaging techniques that need to be addressed: how does technology benefit the patient? It is worth the cost? Is treatment plan enhanced? Is outcome better? Data are necessary for addressing these questions and if appropriate for acceptance among practicing physicians, patients and third party insurers.

The relevance of the proposed study, the CENTURY trial, lies in its original design, testing the impact of stress perfusion imaging by PET coupled with two different intensities of clinical management strategies (standard or comprehensive respectively). This study will examine post-test resource utilization and reduction of cardiovascular risk in patients with known disease or at high risk for CAD.

There will be a total of 1300 men and women enrolled with approximately 650 subjects randomized to one of two treatment arms. Eligible patients must have clinical indications for stress perfusion testing.

Following confirmation of eligibility and provision of signed informed consent, patients will be randomized to one of the two possible treatment strategies. At time of randomization patients will be assigned to "PET guided + comprehensive" versus "standard medical treatment."

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Subjects must be competent to provide written informed consent.
  • Subjects must sign an Institutional Review Board (IRB) approved Informed Consent Form (ICF) and HIPAA Authorization prior to the initiation of any study procedures.
  • Men and women age ≥40
  • _ Indication for stress perfusion testing
  • Appropriate Indications for stress perfusion testing:
  • Suspected CAD:
  • Men with any chest pain syndrome and two other risk factors
  • Women >50 years old with any chest pain syndrome and two other risk factors
  • Asymptomatic men and women >50 years with at least three other risk factors* or Coronary Calcium Agatston score >
  • Diabetic men and women and two other risk factors
  • Documented known CAD:
  • Men and women asymptomatic or stable symptoms and known CAD by abnormal catheterization or prior SPECT without revascularization after >2 years to evaluate worsening disease or
  • Men and women with worsening symptoms and known CAD by abnormal catheterization or prior SPECT/PET without revascularization
  • Men and women with chest pain syndrome and previous revascularization
  • Asymptomatic men and women >5 years after coronary artery bypass graft surgery (CABG) or >2 years after PCI
  • Risk factors: Diabetes, Current or recent cigarette smoking (within the last 12 months), LDL>130, low HDL <50 women, HDL <45 men, history of metabolic syndrome, hypertension (SPB>140), family history of premature (<60 year) CAD, Atherosclerotic carotid artery disease OR atherosclerotic peripheral vascular disease (APVD) as defined by ankle-brachial index below 0.9 and/or by abnormal duplex ultrasound, CT angiography, magnetic resonance angiography (MRA) or conventional invasive angiogram or previous revascularization procedure.
  • Framingham's high risk criteria refers to presence of diabetes mellitus with the limitation described above (c) or 10 year absolute Coronary Heart Disease(CHD)risk of >or= 20% (see tables Appendix A).
  • Chest pain is defined as Typical Angina if Exertional + Retrosternal + relieved with rest or sublingual nitroglycerin (NTG) , Atypical angina if only two of the above criteria are present and Non-anginal if one or none of the above are present.

排除标准

  • Low pretest likelihood of CAD (= not meeting the above criteria)
  • Unstable angina high risk (dynamic ST-Twave ECG changes and/or elevated troponin)
  • Recent MI (<4 weeks)
  • Recent stroke (<4 weeks)
  • CABG or percutaneous coronary intervention (PCI) within the last 6 months
  • Severe renal dysfunction as defined by creatinine > 2.0 mg/dl
  • Active liver disease or hepatic dysfunction, AST or ALT > x 2 the upper limit of normal (ULN)
  • Concomitant valvular heart disease
  • Left ventricular ejection fraction (LVEF) <30%
  • Severe systemic hypertension defined as systolic blood pressure (SBP) > 200 mmHg
  • Symptomatic sustained or non-sustained ventricular tachycardia
  • Morbid Obesity defined by Body Mass Index > 35
  • Sever disability to prevent therapeutic exercise not expected to resolve within 6 months
  • Major non-cardiac co-morbidity limiting survival or social situation/condition that in the opinion of the investigator will preclude the patient from participation in the study follow-up.
  • Concurrent or prior (within last 30 days) participation in other research studies using investigational drugs or devices.

研究组 & 干预措施

Current standard of care

No Intervention

Current standard of care medical management as provided by primary physician.

Intensive lifestyle modification

Experimental

P.E.T. guided comprehensive therapy program. The study intervention is Comprehensive therapy program for risk factor modification. The Comprehensive program of atherosclerotic risk factor modification involves treatment to target lipid levels, blood pressure and diabetes control, smoking cessation, very low fat diet and aerobic exercise program. This is in addition to standard current medical therapy as provided by primary physician. No experimental medications or procedures will be used.

干预措施: Comprehensive therapy program for risk factor modification (Other)

结局指标

主要结局

1.Clinical Endpoints-

时间窗: 2 years, 5 years and 10 years

Average Risk Score modification during 5 year follow-up and major cardiovascular clinical events of death and non-fatal myocardial infarction.

次要结局

  • 2. Secondary outcome(2 years, 5 years and 10 years)

研究者

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

K.Lance Gould

Professor, Internal Medicine, Cardiology

The University of Texas Health Science Center, Houston

研究点 (1)

Loading locations...

相似试验