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临床试验/NCT00213746
NCT00213746已完成不适用

Prediction of Left Ventricular Function Changes Using Low Dose Dobutamine Gated SPECT in Patients Referred for Viability Assessment: The DOGS (DObutamine Gated Spect)Study.

University Hospital, Rouen8 个研究点 分布在 2 个国家目标入组 75 人开始时间: 2003年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
75
试验地点
8

研究概览

简要总结

Viability assessment remains a clinical challenge in patient with coronary artery disease and left ventricular dysfunction. Several imaging modalities are available for evaluating myocardial viability, based either on perfusion or on contractile reserve analysis. Briefly, perfusion analysis is highly sensitive and contractile reserve highly specific. A combined analysis of both perfusion and contractile reserve has been proposed to improve the diagnostic accuracy in patient referred for a revascularization procedure. However, the value of this combined analysis has not been validated in unselected patients referred for viability assessment.

The patients enrolled in the study will undergo a nitrate enhanced rest gated SPECT using a Tc-99m labeled tracer (sestamibi or tetrofosmine) followed by a second gated SPECT acquired during a low-dose dobutamine infusion (10 mcg/kg/mn). All patients will have a 6-month clinical and imaging follow-up, including physical examination and a nitrate enhanced rest gated SPECT using the same radiopharmaceutical. All treatments received during this 6-month period will be recorded, including medical therapy and coronary revascularization (angioplasty, stenting and CABG).

Finally, the value of baseline perfusion and contractile reserve analysis in predicting left ventricular ejection fraction changes at 6-month follow-up will be evaluated.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Documented coronary artery disease
  • •Left ventricular dysfunction (LVEF < 50%)
  • •Patients referred to the Nuclear Medicine department for myocardial viability assessment
  • •Sinus Rhythm
  • •Acceptance of a 6-month follow-up
  • •Signed informed consent

排除标准

  • •Recent acute coronary syndrome (< 21 days)
  • •Atrial Fibrillation or significant arrhythmias
  • •Implanted pacemaker
  • •Contra indication to dobutamine
  • •Non ischaemic cardiomyopathy
  • •Pregnancy

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (8)

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