Regadenoson vs Dipyridamole in Use as Pharmacological Stress Agent Before SPECT
Sponsored by Hospices Civils de Lyon
About this trial
Last updated 7 years ago
Study ID
69HCL17_0056
Status
Completed
Type
Observational
Placebo
No
Accepting
18+ Years
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 8 years ago
What is this trial about?
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.
What are the participation requirements?
Inclusion Criteria
- Adult ≥ 18 years
- Myocardial scintigraphy by pharmacological stress agent
- Used molecules = Dipyridamole or Regadenoson
Exclusion Criteria
- 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