跳至主要内容
临床试验/NCT00449579
NCT00449579Unknown3 期

The Diagnostic Benefits of the HyperQTM System in ECG Stress Testing

Assuta Hospital Systems1 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2006年8月1日最近更新:
适应症

试验速览

阶段
3 期
发起方
入组人数
1,200
试验地点
1
主要终点
ST changes

研究概览

简要总结

The main objective of this study is to determine the usefulness of the HyperQ™ System in improving the positive predictive value of conventional ECG stress testing.

Patients who are referred for stress test will perform an ECG stress test on a treadmill, with high-frequency ECG recording from conventional 12 leads using BSP's HyperQ™ System. Conventional 12 lead ECG, as well as HyperQ™ recordings will be provided by the HyperQ™ System. The results of the conventional test and the HyperQ™ data will be compared, using one of three cardiac tests (stress echocardiography, SPECT myocardial perfusion imaging and angiography) as gold standards.

Statistical analysis will compare the sensitivity, specificity, PPV and NPV of the conventional and HyperQ™ stress ECG in detecting myocardial ischemia.

详细描述

The study population will comprise of 1200 patients referred to stress test in three Maccabi clinics or cardiac medical centers. All patients will perform an ECG stress test with high-frequency ECG recording from conventional 12 leads using BSP's HyperQ™ System. The recording will be done without affecting or interfering with any aspect of the normal due course of the test. Standard Bruce protocol or modified Bruce protocol will be used, with standard test termination indications. Two minutes of rest ECG will be recorded prior to stating the protocol.

Following the test, the physician will interpret the test's results in the conventional manner (e.g. ST changes, chest pain, etc) and decide whether the subject should be referred to additional tests.

HyperQ™ data will be analyzed in two phases: (i) Interpretation by the physician in a non-blinded manner one day following the stress test and (ii) after performing all the exercise tests of the study group, blindly to the conventional diagnosis and the HyperQ™ analysis done previously, as well as to other outcomes of imaging procedures. The first HyperQ™ reading will be used to detect the subjects who were positive according to the HyperQ™ system but negative according to the conventional stress testing. These subjects will be referred by the physician to further clinical investigation. The first reading will also be used to assess the physician's interpretation in a scenario that represents a realistic clinical setting, while the second reading will be used to examine the unbiased clinical benefit of HyperQ™ data.

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
45 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Subject referred to stress ECG
  • •Subjects age ≥ 45
  • •Subject signed an Informed Consent form

排除标准

  • •Subject with contraindications for stress ECG
  • •Subject with implantable pacemaker or defibrillator
  • •Subject with LBBB
  • •Subject with QRS duration ≥ 110 mSec
  • •Subject with Wolff-Parkinson-White Syndrome

结局指标

主要结局

ST changes

HyperQ results

次要结局

未报告次要终点

研究者

发起方
Assuta Hospital Systems
申办方类型
Other

研究点 (1)

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