跳至主要内容
临床试验/NCT03084562
NCT03084562已完成不适用

Descriptive Study Comparing Regadenoson Versus Dipyridamole in Use as Pharmacological Stress Agent Before a Myocardial Perfusion Imaging by Single Photon Emission Computed Tomography (SPECT)

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2017年5月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
300
试验地点
1
主要终点
Duration of the test

研究概览

简要总结

Myocardial perfusion scintigraphy is to evaluate coronary perfusion as well as heart muscle function. This examination takes place in two stages, one imaging at rest and one after a cardiac stress caused. This stress can be triggered as a first-line stress test. A pharmacological stress is proposed when stress test is not possible or contraindicated, Several drugs have a marketing authorization in this indication (adenosine, dipyridamole, regadenoson, dobutamine).

Among them, the regadenoson is the most recent molecule. Marketed in France since 2013, it would allow a reduction of undesirable effects compared to other agents, especially adenosine. It is simple and quick to use thanks to a single dose administration. However, its cost is nearly 30 times higher than dipyridamole. In the investigational center, dipyridamole is currently the first-line pharmacological stress agent, whereas regadenoson is reserved for a limited number of doses, the indication of which must be justified (asthmatic patient or with severe COPD). Few studies in the literature specifically compare these two pharmacological agents (examination time, cost, tolerance) and the opinion on the use of regadenoson in the service is limited.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Adult ≥ 18 years
  • Myocardial scintigraphy by pharmacological stress agent
  • Used molecules = Dipyridamole or Regadenoson

排除标准

  • Physical stress test by single or mixed effort (associating pharmacological stress)
  • Pharmacological agent used = Adenosine
  • Inclusion in the ERCAD protocol
  • Double isotope protocol
  • Patient refusal due to study information

结局指标

主要结局

Duration of the test

时间窗: 24 hours (Visit 1: During the examen)

Evaluate the time savings from the use of regadenoson versus dipyridamole by comparing the duration of the test.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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