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临床试验/EUCTR2007-003492-39-GR
EUCTR2007-003492-39-GR进行中(未招募)不适用

A phase III study to compare SonoVue® enhanced myocardial echocardiography (MCE) to single photon emission computerized tomography (ECG-GATED SPECT), at rest and at peak of low-dose Dipyridamole stress test, in the assessment of significant coronary artery disease (CAD) in patients with suspect or known CAD using Coronary Angiography as Gold Standard - SonoVue MCE vs SPECT

Bracco Imaging S.p.A.0 个研究点目标入组 597 人开始时间: 2009年1月30日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
597

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Include subjects of both sexes who fulfill all following inclusion criteria:
  • ·Having at least 18 years of age.
  • ·Having a known or suspected coronary artery disease (CAD) indicated for stress ECG-gated SPECT and coronary angiography to clarify whether they have a clinical significant coronary stenosis (=70%).
  • ·Having provided written Informed Consent and willing to comply with protocol requirements.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclude a subject from this study if the subject does not fulfill the inclusion criteria, or if any of the following conditions are observed:
  • ·Has any clinically unstable cardiac condition prior to SonoVue® administration such as:
  • ·evolving or ongoing myocardial infarction,
  • ·a history of acute myocardial infarction or PCI within the previous 3 months,
  • ·worsening of typical angina at rest within the previous 7 days,
  • ·significant worsening of cardiac symptoms within the previous 7 days,
  • ·recent coronary artery intervention or other factors suggesting clinical instability (e.g., recent deterioration of ECG, laboratory or clinical findings),
  • ·acute cardiac failure, class III/IV cardiac failure,
  • ·severe cardiac rhythm disorders (ventricular tachycardia sustained and not sustained in combination with symptoms).
  • ·Has any contra-indications to dipyridamole or aminophylline (e.g. hypersensitivity to xanthines) according to each agent’s package insert.
  • ·Has any known allergy to one or more of the ingredients of the investigational product.
  • ·Has a previous Coronary Artery By-pass.
  • ·Has any revascularization procedure or change of clinical status that may warrant a change in their status of CAD among the clinical testing under evaluation (coronary angiography, MCE or ECG-GATED SPECT).
  • ·Has used methylated xanthines (chocolate, caffeine – including coffee, tea, and cola drinks), phosphodiesterase inhibitor drugs such as aminophylline or dipyridamole within 24 hours prior SonoVue® enhanced echocardiography or SPECT.
  • ·Has not visualization of left ventricle at basal echocardiography.
  • ·Has received an investigational compound within 30 days before admission into this study.
  • ·Has any medical condition or other circumstances which would significantly decrease the chances of obtaining reliable data, achieving study objectives, or completing the study and/or post dose follow-up examinations.
  • ·Is determined by the Investigator that the subject is clinically unsuitable for the study.
  • ·Is a pregnant or lactating female. Exclude the possibility of pregnancy:
  • ·by testing on site at the institution (serum or urine ßHCG) within 24 hours prior to the start of investigational product administration,
  • ·by surgical history (e.g., tubal ligation or hysterectomy),
  • ·post menopausal with a minimum 1 year without menses.

研究者

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A phase III study to compare SonoVue® enhanced... | 临床试验